FDA Recalls - April 2026 (714 reports)
FDA Recalls issued during April 2026.
FDA Recalls
FDA Recall of MicroScan Neg Multidrug Resistant MIC 1 by Beckman Coulter
FDA ·
FDA Recalls high
FDA Issues Recall for Spacelabs Multi-parameter Command Module
FDA ·
FDA Recalls high
FDA Recall of Medline Medical Convenience Kits Due to Syringe Risk
FDA ·
FDA Recalls
Recall of Cook Medical Cook Staged Extubation Set Over Expiration Date Issue
FDA ·
FDA Recalls
Cook Medical Central Venous Catheter Tray Recall
FDA ·
FDA Recalls high
Medline Medical Kits Recall Over Syringe Connection Risk
FDA ·
FDA Recalls high
Medline Industries Recalls Angiographic Syringes
FDA ·
FDA Recalls
Recall of COOK MEDICAL Wayne Pneumothorax Tray Due to Incorrect Expiration Dates
FDA ·
FDA Recalls high
Recall of Medline Medical Convenience Kits Due to Syringe Risk
FDA ·
FDA Recalls high
Recall of Medline TAVR PACK Medical Kits
FDA ·
FDA Recalls
Cook Medical Approach CTO-12 Micro Wire Guide Recall
FDA ·
FDA Recalls
Recall of Cook Medical NCompass Nitinol Stone Extractor for Expiration Date Issue
FDA ·
FDA Recalls
Cook Medical Ciaglia Blue Rhino Tracheostomy Introducer Set Recall
FDA ·
FDA Recalls
COOK MEDICAL Multipurpose Drainage Catheter Recall
FDA ·
FDA Recalls
Recall of Cook Medical Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Sets
FDA ·
FDA Recalls
Tornier HRS Max Parts Recall
FDA ·
FDA Recalls
Recall of See Luer Cap Set by Molded Products Inc
FDA ·
FDA Recalls high
Recall of Medline Medical Convenience Kits Due to Connection Risk
FDA ·
FDA Recalls
FDA Recall of MicroScan Neg MIC 3J by Beckman Coulter
FDA ·
FDA Recalls
Recall of Cook Medical Thal-Quick Chest Tube Tray Due to Incorrect Expiration Dates
FDA ·
FDA Recalls
FDA Recall of Cook Medical Approach CTO-6 Micro Wire Guide
FDA ·
FDA Recalls
Cook Medical Spectrum Central Venous Catheter Set Recall
FDA ·
FDA Recalls
FDA Mandated Recall of Siemens ARTIS Pheno and Icono Systems
FDA ·
FDA Recalls
Cook Medical Spectrum Central Venous Tray Recall
FDA ·
FDA Recalls
Stryker Sustainability Solutions Recall for Tourniquet Cuffs
FDA ·
FDA Recalls
Recall of B.R.A.H.M.S PlGF Plus KRYPTOR Diagnostic Test
FDA ·
FDA Recalls
Recall of COOK MEDICAL Approach CTO-18 Micro Wire Guide for Incorrect Expiration Dates
FDA ·
FDA Recalls high
Medline Industries Recall of NAMIC Angiographic Syringes
FDA ·
FDA Recalls
FDA Recall of Cook Medical Blue Rhino G2-Multi Tracheostomy Introducer Tray
FDA ·
FDA Recalls
Recall of COOK MEDICAL Wayne Pneumothorax Set Due to Incorrect Expiration Dates
FDA ·
FDA Recalls
Recall of Cook Medical Cook Strange Bile Duct Stone Exploration Set
FDA ·
FDA Recalls
Recall of Melker Universal Cuffed Emergency Cricothyrotomy Catheter Set
FDA ·
FDA Recalls high
Recall of Medline Medical Convenience Kits
FDA ·
FDA Recalls high
Medline Medical Convenience Kits Recall
FDA ·
FDA Recalls high
Medline NAMIC Angiographic Control Syringes Recall Over Connection Risk
FDA ·
FDA Recalls
FDA Recall of Cook Medical Arterial Pressure Monitoring Tray Due to Incorrect Expiration Dates
FDA ·
FDA Recalls high
Medline Medical Convenience Kits Recall Over Syringe Connection Risk
FDA ·
FDA Recalls
Recall of XTANT Medical Xpress Pedicle Screw System
FDA ·
FDA Recalls
Recall of Vital Nutrients Aller-C Due to Undeclared Allergens
FDA ·
FDA Recalls
Recall of ReadyMeals Turkey Bacon & Cheddar Pretzel Duo Sandwich Due to Undeclared Sesame
FDA ·
FDA Recalls high
FDA Recall of Boner Bears Honey Male Enhancement Announced
FDA ·
FDA Recalls
Zarlengo's Chocolate Gelato Recall Due to Labeling Issue
FDA ·
FDA Recalls
Recall of Olive Skewers Due to Banned Sweetener
FDA ·
FDA Recalls high
FDA Recall of Red Bull Extreme Male Enhancement Supplement
FDA ·
FDA Recalls
Recall of DADI NONGFU Dried Salt Chilli Vegetable(S) by MEI YU CHENG DA TRADING INC
FDA ·
FDA Recalls high
FDA Recall of Blue Bull Extreme Male Enhancement Supplement
FDA ·
FDA Recalls
Recall of Riverence Smoked Trout Dip Due to Labeling Issue
FDA ·
FDA Recalls
Recall of Zarlengo's Chocolate Chocolate Chip Gelato for Allergen Issue
FDA ·
FDA Recalls high
FDA Issues Recall for Connecticut Crab Company Crab Cakes
FDA ·
FDA Recalls
Lanreotide Acetate Injection Recall by Cipla USA
FDA ·
FDA Recalls
Recall of 0.9% Sodium Chloride Injection by BD
FDA ·
FDA Recalls
Isotretinoin Capsules Recall by Teva Pharmaceuticals
FDA ·
FDA Recalls
Recall of GE Healthcare's Omnipaque Injection Due to Particulate Matter
FDA ·
FDA Recalls
Recall of Vancomycin HCL Injection by Fagron Compounding Services
FDA ·
FDA Recalls
Teva Pharmaceuticals Recalls Isotretinoin Capsules Over Potency Concerns
FDA ·
FDA Recalls
Recall of Sodium Chloride Injection by Fresenius Kabi
FDA ·
FDA Recalls
Recall of 0.9% Sodium Chloride Injection Due to Sterility Concerns
FDA ·
FDA Recalls
FDA Recall of Norepinephrine Bitartrate Injection by Fagron Compounding Services
FDA ·
FDA Recalls
FDA Recall of Artificial Tears Eye Drops Due to Sterility Concerns
FDA ·
FDA Recalls
Xanax XR Tablets Recall Over Failed Dissolution Specifications
FDA ·
FDA Recalls
Recall of Fresenius Kabi 0.9% Sodium Chloride Injection
FDA ·
FDA Recalls
Recall of Dextrose Injection by Fresenius Kabi USA
FDA ·
FDA Recalls
FDA Recall of Fresenius Kabi Dextrose Injection
FDA ·
FDA Recalls
FDA Recall of Clonidine Transdermal System Due to Manufacturing Issue
FDA ·
FDA Recalls
Recall of Fresenius Kabi 5% Dextrose Injection Due to Sterility Concerns
FDA ·
FDA Recalls
FDA Recall of Sodium Chloride Injection Due to Sterility Concerns
FDA ·
FDA Recalls high
FDA Recall of Vancomycin HCI Injection by Fagron Compounding Services
FDA ·
FDA Recalls
Recall of Clonidine Transdermal System Due to Manufacturing Issue
FDA ·
FDA Recalls
FDA Recall of Fresenius Kabi's Sodium Chloride Injection
FDA ·
FDA Recalls
Recall of Fresenius Kabi Sodium Chloride Injection
FDA ·
FDA Recalls
Fresenius Kabi Sodium Chloride Injection Recall
FDA ·
FDA Recalls
Clonidine Transdermal System Recall Over Manufacturing Issue
FDA ·
FDA Recalls
FDA Recall of Fresenius Kabi Sodium Chloride Injection
FDA ·
FDA Recalls
Fagron Compounding Services Issues Recall for Vancomycin HCI Injection
FDA ·
FDA Recalls
Philips Azurion 7 B12 Recall for X-ray Imaging Issues
FDA ·
FDA Recalls
FDA Recall of Synthes 2.4 VOLT(TM) TAP CORTEX SCREW
FDA ·
FDA Recalls
Recall of Philips Allura Xper FD10C Systems
FDA ·
FDA Recalls high
Recall of Medline Anterior Hip Pack Due to Safety Issue
FDA ·
FDA Recalls high
FDA Recall of Medtronic MiniMed 700G Insulin Pump for Delivery Issues
FDA ·
FDA Recalls
Recall of Paradise Catheter by ReCor Medical Inc.
FDA ·
FDA Recalls
FDA Announces Recall of Philips Vue Motion V12 Medical Device
FDA ·
FDA Recalls
Philips Azurion 7 M20 Recall for X-ray Imaging Issues
FDA ·
FDA Recalls
Philips ALLURA Xper FD20 Recall for Imaging Issues
FDA ·
FDA Recalls
Burlington Medical BAT Coverage Recall
FDA ·
FDA Recalls
FDA Recall of da Vinci S, Si Tenaculum Forceps Instrument
FDA ·
FDA Recalls
Burlington Medical Kilt Recall Over Attenuation Degradation
FDA ·
FDA Recalls
FDA Recall of Philips Allura Xper FD20/20 Systems
FDA ·
FDA Recalls
Recall of Philips Allura Xper FD20/15 Medical Device
FDA ·
FDA Recalls high
FDA Recall of Philips Respironics Trilogy Evo Ventilator
FDA ·
FDA Recalls
Burlington Medical Caps Recall
FDA ·
FDA Recalls high
FDA Recall of Medline Kits Containing Olympus Biopsy Valves
FDA ·
FDA Recalls
Stryker CHROMOPHARE Softlit Ring Surgical Light System Recall
FDA ·
FDA Recalls
Recall of Philips ALLURA Xper FD10 OR Table for Imaging Issues
FDA ·
FDA Recalls
Burlington Medical Thyroid Shield Recall
FDA ·
FDA Recalls
Recall of eTRAX Needle System Starter Kit by Civco Medical Instruments
FDA ·
FDA Recalls
Recall of Philips ALLURA Xper FD10/10 Medical Devices
FDA ·
FDA Recalls high
Recall of Medtronic MiniMed 770G Insulin Pumps for Delivery Issues
FDA ·
FDA Recalls
Recall of da Vinci S, Si Double Fenestrated Grasper Instrument
FDA ·
FDA Recalls
Medline Industries Recalls Sterile Radiology Procedure Kits
FDA ·
FDA Recalls
FDA Recall of Finesse BTK Multicath by SUMMA THERAPEUTICS
FDA ·
FDA Recalls
Recall of Olympus SOLTIVE Pro Laser System Due to Power Supply Defect
FDA ·
FDA Recalls high
Medline Convenience Kits Recall Over Biopsy Valve Issue
FDA ·
FDA Recalls
FDA Recall of Philips Allura Xper FD20/20 OR Table
FDA ·
FDA Recalls high
FDA Recall of Philips Respironics Trilogy EV300 Ventilator
FDA ·
FDA Recalls high
Baxter Healthcare Recall of Blue Ventilator Adapter Module
FDA ·
FDA Recalls
Philips Azurion 5 M20 Device Recall
FDA ·
FDA Recalls
FDA Recall of eTRAX Needle Sensor for Aurora Trackers
FDA ·
FDA Recalls
Recall of da Vinci S and Si Monopolar Curved Scissors Instrument
FDA ·
FDA Recalls
Recall of Artoura Breast Tissue Expanders Due to Needle Issue
FDA ·
FDA Recalls
Recall of Burlington Medical Blockers Due to Attenuation Degradation
FDA ·
FDA Recalls high
Recall of Philips Respironics Trilogy Evo Universal Ventilator
FDA ·
FDA Recalls
FDA Recall of CPX 4 US Breast Tissue Expanders Due to Needle Issues
FDA ·
FDA Recalls high
FDA Recall of Medtronic MiniMed 630G Insulin Pump
FDA ·
FDA Recalls high
Recall of RefleXion X1 Radiotherapy System Due to Software Defect
FDA ·
FDA Recalls
Philips Azurion 7 M12 Recall Due to X-ray Imaging Issues
FDA ·
FDA Recalls high
Medtronic MiniMed 640G Insulin Pump Recall
FDA ·
FDA Recalls high
Medtronic MiniMed 780G Insulin Pump Recall Over Delivery Issues
FDA ·
FDA Recalls
Philips Azurion 3 M15 Recall for X-ray Imaging Issues
FDA ·
FDA Recalls
Recall of Burlington Medical Frontal Aprons for Attenuation Degradation
FDA ·
FDA Recalls high
FDA Recall of Medtronic MiniMed 530G Insulin Pump
FDA ·
FDA Recalls
Recall of Jiffy Original Composite Polisher Cups
FDA ·
FDA Recalls high
Medline Kits Recall Involving Olympus Biopsy Valves
FDA ·
FDA Recalls
FDA Recall of Paradise Ultrasound Renal Denervation System
FDA ·
FDA Recalls
Recall of eTRAX Needle Sensor Due to Inspection Error
FDA ·
FDA Recalls
Philips ALLURA Xper FD20 OR Table Recall
FDA ·
FDA Recalls
FDA Recall of Medline's ENFIT G-TUBE Connector
FDA ·
FDA Recalls
Recall of da Vinci S, Si Grasping Retractor Instrument
FDA ·
FDA Recalls
Burlington Medical Protective Sleeves Recall
FDA ·
FDA Recalls
FDA Recall of Artoura Breast Tissue Expanders Due to Needle Issues
FDA ·
FDA Recalls
Philips Allura Xper FD20/10 Device Recall
FDA ·
FDA Recalls
Recall of CPX 4 US Breast Tissue Expanders Issued by FDA
FDA ·
FDA Recalls high
Medline Bronchoscopy Kits Recall
FDA ·
FDA Recalls
FDA Recall of Burlington Medical Kilt Blockers Due to Attenuation Degradation
FDA ·
FDA Recalls
Medline Kits with ENFIT G-TUBE Connector Recall
FDA ·
FDA Recalls high
Recall of Medtronic Paradigm REAL-Time Revel Insulin Pumps
FDA ·
FDA Recalls
FDA Recall of CPX 4 US Breast Tissue Expanders
FDA ·
FDA Recalls
Recall of Siemens Atellica CH A1c_E Devices for Potential Result Errors
FDA ·
FDA Recalls
Recall of Philips ALLURA Xper FD10F Medical Device
FDA ·
FDA Recalls
Recall of Burlington Medical Demi Half Aprons Due to Attenuation Degradation
FDA ·
FDA Recalls
Recall of Olympus SOLTIVE Laser System Due to Power Supply Defect
FDA ·
FDA Recalls
Recall of Philips ALLURA Xper FD20 Biplane OR Table for Imaging Issues
FDA ·
FDA Recalls high
Abiomed Impella Controller Recall for Alarm Delay Issue
FDA ·
FDA Recalls high
Medtronic MiniMed 740G Insulin Pump Recall
FDA ·
FDA Recalls
FDA Recall of Burlington Medical Vests Due to Attenuation Degradation
FDA ·
FDA Recalls
Recall of Burlington Medical Half Aprons for Attenuation Degradation
FDA ·
FDA Recalls
Recall of eTRAX Needle System Starter Kit 14G Due to Programming Error
FDA ·
FDA Recalls
Recall of Oxoid Microbact Identification Kits for Listeria
FDA ·
FDA Recalls
Philips Azurion 5 M12 Recall Over X-ray Imaging Issues
FDA ·
FDA Recalls
FDA Recall of Civco Medical's eTRAX Needle Sensor
FDA ·
FDA Recalls high
Recall of Medtronic Paradigm Insulin Pumps
FDA ·
FDA Recalls high
FDA Recall of Medline Airway Exam Kit
FDA ·
FDA Recalls
Philips Azurion 7 B20 Systems Recall Issued
FDA ·
FDA Recalls
FDA Recall of eTRAX Needle System Starter Kit 16G Announced
FDA ·
FDA Recalls
Philips Azurion 3 M12 Recall for X-ray Imaging Issues
FDA ·
FDA Recalls
FDA Recall of BD Kiestra ReadA Devices
FDA ·
FDA Recalls
Synthes 2.4 VOLT TAP LOCKING SCREW TAP Recall Due to Thread Issue
FDA ·
FDA Recalls high
Recall of Medtronic MiniMed 620G Insulin Pump for Delivery Issues
FDA ·
FDA Recalls
FDA Recall of CPX 4 US Breast Tissue Expanders Due to Needle Issue
FDA ·
FDA Recalls
Recall of eTRAX Needle Sensor by Civco Medical Instruments
FDA ·
FDA Recalls
Recall of Philips Allura Xper FD20/15 OR Table Due to Imaging Issues
FDA ·
FDA Recalls
Recall of da Vinci S, Si Mega Needle Driver Instrument Due to Cable Issues
FDA ·
FDA Recalls
Recall of Burlington Medical Leg Wraps Due to Attenuation Degradation
FDA ·
FDA Recalls high
Medtronic MiniMed Paradigm REAL-Time Veo Insulin Pump Recall
FDA ·
FDA Recalls
Recall of Philips ALLURA Xper FD20 Biplane Systems
FDA ·
FDA Recalls
Burlington Medical Wrap Aprons Recall Due to Attenuation Degradation
FDA ·
FDA Recalls high
Recall of Medtronic MiniMed Paradigm REAL-Time Insulin Pumps
FDA ·
FDA Recalls
FDA Recall of eTRAX Needle System Starter Kit
FDA ·
FDA Recalls high
Recall of Medtronic MiniMed 720G Insulin Pump
FDA ·
FDA Recalls
Recall of da Vinci S, Si Permanent Cautery Hook Instrument
FDA ·
FDA Recalls
GE Healthcare LLC Announces Recall of SIGNA Premier Systems
FDA ·
FDA Recalls high
Recall of THORACIC ROBOTS DYNJ908777B by Medline Industries
FDA ·
FDA Recalls
FDA Recall of MEI HEONG YUEN Garlic Flavor Roasted Peanuts
FDA ·
FDA Recalls
FDA Recall of MEI HEONG YUEN Walnut Flavor Roasted Peanuts Due to Banned Sweetener
FDA ·
FDA Recalls
FDA Announces Recall of Imu-Tek Colostrum-5 Powder
FDA ·
FDA Recalls
FDA Announces Recall of Divided Sunset Multi Collagen Peptides
FDA ·
FDA Recalls
HEYTEA USA Inc. Recalls Coconut Drink 1 Over Undeclared Milk
FDA ·
FDA Recalls
Recall of MEI HEONG YUEN Tangerine Flavor Roasted Peanuts
FDA ·
FDA Recalls
FDA Recall of Imu-Tek Colostrum-5 Capsules Announced
FDA ·
FDA Recalls
FDA Recall of Mama Rose's Prickly Pear Salad Dressing Due to Undeclared Sulfites
FDA ·
FDA Recalls
FDA Recall of Pocas International's Popping Boba RTD Peach Oolong Tea
FDA ·
FDA Recalls
Recall of POPPING BOBA RTD MANGO PASSION FRUIT GREEN TEA
FDA ·
FDA Recalls
Recall of POPPING BOBA RTD STRAWBERRY DRAGON F/OOLONG TEA
FDA ·
FDA Recalls
FDA Recall of JFE Franchising Dumpling Products Due to Glass Contamination
FDA ·
FDA Recalls
Recall of POPPING BOBA RTD MIXED BERRY HIBISCUS TEA by Pocas International Corp.
FDA ·
FDA Recalls
Recall of Dumpling Vegetable Products by JFE Franchising Inc.
FDA ·
FDA Recalls high
FDA Recall of Lone Star Dairy Products' Spray Dried Dairy Powder Due to Salmonella
FDA ·
FDA Recalls
Prickly Pear Jelly Recall by The Maros Group Due to Undeclared Milk
FDA ·
FDA Recalls
Recall of Sterile Eye Drops by K.C. Pharmaceuticals Due to Sterility Concerns
FDA ·
FDA Recalls
Recall of Various Eye Drops Due to Sterility Concerns
FDA ·
FDA Recalls
FDA Recall of Various Eye Drop Brands Over Sterility Concerns
FDA ·
FDA Recalls
FDA Recall of Prazosin Hydrochloride Capsules by Biocon Pharma
FDA ·
FDA Recalls high
Recall of Magnesium Sulfate in Water for Injection by Amneal Pharmaceuticals
FDA ·
FDA Recalls high
Recall of Various Eye Drop Brands Due to Sterility Concerns
FDA ·
FDA Recalls
Recall of Artificial Tears and Other Eye Drops Announced
FDA ·
FDA Recalls
Recall of Multiple Eye Drop Brands Due to Sterility Concerns
FDA ·
FDA Recalls
FDA Announces Recall of Ultra Lubricating Eye Drops
FDA ·
FDA Recalls
Recall of Artificial Tears Eye Drops Due to Sterility Concerns
FDA ·
FDA Recalls
FDA Announces Recall of Prazosin Hydrochloride Capsules
FDA ·
FDA Recalls
FDA Recalls Tramadol Hydrochloride Tablets Over Impurity Issue
FDA ·
FDA Recalls
Recall of Prazosin Hydrochloride Capsules Due to Impurity Concerns
FDA ·
FDA Recalls high
Recall of Philips Respironics Trilogy Evo Ventilator
FDA ·
FDA Recalls high
Recall of Puracol and Puracol Plus Collagen Wound Dressings
FDA ·
FDA Recalls
FDA Recall of Pelvic Reconstruction System by I.T.S. GmbH
FDA ·
FDA Recalls
Recall of Philips L12-5 Ultrasound Transducer
FDA ·
FDA Recalls
Recall of Olympus HALO PKS Cutting Forceps Due to Welding Defect
FDA ·
FDA Recalls
FDA Recall of MicroScan Neg MIC 56 Due to Contamination
FDA ·
FDA Recalls high
FDA Recall of Volar Radius Plate by I.T.S. GmbH
FDA ·
FDA Recalls high
FDA Class I Recall for Erbe USA Inc's Flexible Cryoprobe
FDA ·
FDA Recalls
FDA Recall for Philips C9-4 Ultrasound Transducer
FDA ·
FDA Recalls
BiDop 3 Pocket Doppler Recall Issued by FDA
FDA ·
FDA Recalls
FDA Recall of Olympus PKS Cutting Forceps Due to Welding Defect
FDA ·
FDA Recalls
Recall of Olympus Everest Bipolar Cutting Forceps
FDA ·
FDA Recalls
Recall of I.T.S. GmbH Pilon Plates Over MRI Safety Concerns
FDA ·
FDA Recalls
FDA Recall of Philips X7-2 Ultrasound Transducer
FDA ·
FDA Recalls
Recall of Philips 3D6-2 Ultrasound Transducer
FDA ·
FDA Recalls high
Recall of FR.O.H. Calcaneus Repair System Due to MRI Safety Concerns
FDA ·
FDA Recalls
Recall of Straumann Custom Abutment AS Ti Due to Manufacturing Mix-Up
FDA ·
FDA Recalls
FDA Recall of Embrace Drill Tower Due to Labeling Error
FDA ·
FDA Recalls
FDA Announces Recall of I.T.S. DUL and UOL Systems
FDA ·
FDA Recalls
Recall of Philips OMNI III TEE Ultrasound Transducer Announced
FDA ·
FDA Recalls
Recall of Philips Mini Multi TEE Ultrasound Transducer
FDA ·
FDA Recalls
Recall of Humeral Head Plate Devices by I.T.S. GmbH
FDA ·
FDA Recalls high
Recall of DuraMax Chronic Hemodialysis Catheter Announced
FDA ·
FDA Recalls high
I.T.S. GmbH Clavicula Plate Recall Over MRI Safety Concerns
FDA ·
FDA Recalls
Recall of Olympus Everest Bipolar Cutting Forceps Model 3005
FDA ·
FDA Recalls
Recall of TECNIS Eyhance IOL with Delivery System
FDA ·
FDA Recalls
I.T.S. GmbH Fibula Plate Recall
FDA ·
FDA Recalls
Recall of Straumann Custom Abutment Ti Devices
FDA ·
FDA Recalls
FDA Recall of Olympus Endoscope Air/Water Valve MAJ-1444
FDA ·
FDA Recalls high
FDA Recall of Handy Solutions Neck & Shoulders Heating Pad
FDA ·
FDA Recalls high
Recall of BioFlo DuraMax Catheters Due to Design Defect
FDA ·
FDA Recalls
Recall of Philips L17-5 Ultrasound Transducer for Labeling Clarification
FDA ·
FDA Recalls
I.T.S. LRS Locking System Recall Due to MRI Safety Concerns
FDA ·
FDA Recalls
Recall of Olympus Endoscope Reprocessor OER-Elite
FDA ·
FDA Recalls
FDA Recall of Tandem Insulin Pumps Due to User Guide Errors
FDA ·
FDA Recalls high
Recall of Merit Medical's 16F Dual Valved Splittable Sheath Introducer
FDA ·
FDA Recalls
FDA Recall of Olympus PK Cutting Forceps Due to Welding Defect
FDA ·
FDA Recalls
Recall of Philips OMNI II TEE Ultrasound Transducer
FDA ·
FDA Recalls
FDA Announces Recall of Philips X3-1 Ultrasound Transducer
FDA ·
FDA Recalls
FDA Recall of Olympus Endoscope Reprocessor OER-Pro
FDA ·
FDA Recalls high
Recall of Philips Respironics Trilogy Evo O2 Ventilator for Safety Issue
FDA ·
FDA Recalls
Recall of Imactis CT-Navigation System by GE Medical Systems
FDA ·
FDA Recalls
FDA Recall of Philips S4-1 Ultrasound Transducer
FDA ·
FDA Recalls high
Recall of ProGuide Chronic Dialysis Catheters Due to Design Defect
FDA ·
FDA Recalls
Recall of Olympus Endoscope Suction Valve MAJ-1443
FDA ·
FDA Recalls
Recall of I.T.S. Pelvic Reconstruction System Over MRI Safety Concerns
FDA ·
FDA Recalls high
I.T.S. Straight Plate Recall Due to MRI Safety Issues
FDA ·
FDA Recalls high
FDA Recall of Flexible Cryoprobe by Erbe USA Inc
FDA ·
FDA Recalls high
FDA Recall of CentrosFLO Hemodialysis Catheters Due to Design Defect
FDA ·
FDA Recalls
Recall of Distal Humeral Plates by I.T.S. GmbH
FDA ·
FDA Recalls
Recall of HLS Hand Locking Plates System by I.T.S. GmbH
FDA ·
FDA Recalls
Recall of Olympus PKS Cutting Forceps Due to Welding Defect
FDA ·
FDA Recalls high
I.T.S. Screw System Recall Due to MRI Safety Concerns
FDA ·
FDA Recalls
Recall of Philips S5-2 Ultrasound Transducer Issued
FDA ·
FDA Recalls
FDA Recall of Olecranon Plates by I.T.S. GmbH
FDA ·
FDA Recalls high
Recall of Flexible Cryoprobe by Erbe USA Inc
FDA ·
FDA Recalls
Recall of I.T.S. GmbH Foot Locking Plates and Hallux Osteotomy Plates
FDA ·
FDA Recalls high
Recall of Philips Respironics Trilogy Evo Universal Ventilators
FDA ·
FDA Recalls
Recall of HCS Headless Compression Screw System by I.T.S. GmbH
FDA ·
FDA Recalls
FDA Recall of Orthalign Drill Plate Due to Manufacturing Issue
FDA ·
FDA Recalls
FDA Issues Recall for Orthalign Drill Plate Due to Manufacturing Defect
FDA ·
FDA Recalls
Recall of Pepsin 1:10,000 Powder Due to Potential Salmonella Contamination
FDA ·
FDA Recalls
FDA Recall of Bulk Packaged Colustrum Powder by Herbal Creations USA
FDA ·
FDA Recalls
Recall of King Harvest Sundried Tomato Hummus Due to Foreign Material
FDA ·
FDA Recalls
Recall of King Harvest Spinach Hummus Due to Foreign Material
FDA ·
FDA Recalls high
Nuts.com Recalls Espresso Malted Milk Balls Over Undeclared Allergens
FDA ·
FDA Recalls high
FDA Recall of Doraditas de Azucar Over Allergen Labeling Issue
FDA ·
FDA Recalls
FDA Recall of Tops GOLD Khatta Meetha Pickle Due to Potential Adulteration
FDA ·
FDA Recalls
Basil Pesto & Mozzarella Pizza Recall Due to Metal Fragments
FDA ·
FDA Recalls
Recall of Pepsin Full Strength Powder Due to Potential Salmonella Contamination
FDA ·
FDA Recalls
Slow Roasted Diced Tomatoes Recall Due to Metal Fragments
FDA ·
FDA Recalls
Recall of Ajinomoto Vegetable Gyoza Dumplings Due to Glass Contamination
FDA ·
FDA Recalls
FDA Recall of King Harvest Balsamic Hummus Due to Aluminum Pieces
FDA ·
FDA Recalls
Recall of Sevillo Fine Foods' Slow Roasted Diced Tomatoes Due to Metal Fragments
FDA ·
FDA Recalls high
Recall of Gorditas de Azucar Due to Missing Allergen Labels
FDA ·
FDA Recalls
Recall of Ajinomoto Japanese-Style Vegetable Fried Rice Due to Glass Contamination
FDA ·
FDA Recalls
Recall of First Street Chilli Spanish Peanuts Due to Glass Contamination
FDA ·
FDA Recalls
FDA Recall of Tops GOLD Mango Pickle Due to Potential Adulteration
FDA ·
FDA Recalls
Ajinomoto Teppanyaki Style Vegetable Fried Rice Recall
FDA ·
FDA Recalls
Recall of King Harvest Jalapeno Hummus Due to Aluminum Pieces
FDA ·
FDA Recalls
Recall of Tops GOLD Lime Pickle Due to Potential Adulteration
FDA ·
FDA Recalls
Sunflour Bakery Hamburger Bun Recall
FDA ·
FDA Recalls
Recall of Ajinomoto Golden Tiger Vegetable Fried Rice Due to Glass Contamination
FDA ·
FDA Recalls
FDA Recall of King Harvest Black Olive Hummus Due to Foreign Material
FDA ·
FDA Recalls
Trader Joe's Japanese Style Fried Rice Recall Due to Glass Contamination
FDA ·
FDA Recalls
Recall of Pan de Bono Cheese Bread Due to Undeclared Soy
FDA ·
FDA Recalls
Kroger Chinese Inspiration Vegetable Fried Rice Recall Due to Glass Contamination
FDA ·
FDA Recalls
Recall of Savannah Bee Company Honey BBQ Sauce Mustard Due to Undeclared Allergens
FDA ·
FDA Recalls
Recall of Roasted Tomato Parmesan Focaccia Bread Due to Metal Fragments
FDA ·
FDA Recalls
Recall of King Harvest Roasted Red Pepper Hummus Due to Aluminum Pieces
FDA ·
FDA Recalls
Recall of Pepsin 1:3000 Powder Due to Potential Salmonella Contamination
FDA ·
FDA Recalls
Recall of Treasured Harvest Chilli Spanish Peanuts Due to Glass Contamination
FDA ·
FDA Recalls
FDA Recall of Lucerne 2% Cottage Cheese Due to Metal Fragments
FDA ·
FDA Recalls
Recall of Tops GOLD Mixed Pickle Due to Potential Erucic Acid Adulteration
FDA ·
FDA Recalls
Trader Joe's Vegetable Fried Rice Recall
FDA ·
FDA Recalls
Ajinomoto Tai Pei Shrimp Fried Rice Recall Due to Glass Contamination
FDA ·
FDA Recalls high
Recall of SiluetaYa Mexican Tejocote Roots Supplement Due to Toxic Substance
FDA ·
FDA Recalls
Ajinomoto Vegetable Gyoza Dumplings Recall Due to Glass Contamination
FDA ·
FDA Recalls
FDA Recall of Tops GOLD Green Chilli Pickle Due to Potential Adulteration
FDA ·
FDA Recalls
FDA Recall of Rose and Shore 14" Margarita Thin Crust Pizza Due to Potential Metal Contamination
FDA ·
FDA Recalls
FDA Recall of Ajinomoto Ling Ling Fried Rice Due to Glass Contamination
FDA ·
FDA Recalls
Recall of Ajinomoto Green Gyoza Dumplings Due to Glass Contamination
FDA ·
FDA Recalls
Recall of Tops GOLD Stuffed Red Chilli Pickle Due to Potential Adulteration
FDA ·
FDA Recalls
Recall of CUROSURF Drug by Chiesi USA Due to Sterility Concerns
FDA ·
FDA Recalls
Recall of Sodium Iodide I-131 Due to Failed Specifications
FDA ·
FDA Recalls
FDA Issues Recall for Meclizine Hydrochloride Tablets
FDA ·
FDA Recalls
Recall of Octreotide Acetate Injection by Teva Pharmaceuticals
FDA ·
FDA Recalls
FDA Recall of Levothyroxine Sodium Tablets Due to Subpotency
FDA ·
FDA Recalls
Agebox Recalls iKids-Growth Capsules Due to Undeclared Ibutamoren
FDA ·
FDA Recalls high
Agebox Recalls iKids-Growth Night Formula Due to Undeclared Ibutamoren
FDA ·
FDA Recalls
Agiliti Health Recalls Adapt Pump Support Surfaces Due to Software Malfunction
FDA ·
FDA Recalls
Auris Health Recalls MONARCH Bronchoscopy Platform Due to Software Malfunction
FDA ·
FDA Recalls
AvKARE Issues Voluntary Recall for Amantadine HCl Capsules Due to Dissolution Failure
FDA ·
FDA Recalls
Bard Peripheral Vascular Recalls Hickman and Broviac Catheter Trays Over Sterility Risks
FDA ·
FDA Recalls high
Baxter Healthcare Recalls Spectrum IQ Infusion Pumps Due to Missing Safety Testing
FDA ·
FDA Recalls high
BioGlo Fluorescein Sodium Ophthalmic Strips Recalled Due to Sterility Concerns
FDA ·
FDA Recalls
Centinel Spine Recalls Prodisc C SK Cervical Disc Replacement Devices Due to Mislabeled Sizing
FDA ·
FDA Recalls
Edermy LLC Issues Recall for PIE Trolley System Model 2005 Due to Lack of FDA Clearance
FDA ·
FDA Recalls
Edermy LLC Recalls PIE PAK Medical Devices Due to Lack of 510K Clearance
FDA ·
FDA Recalls
Encore Medical, LP Recalls Reverse Shoulder Prosthesis Humeral Socket Inserts Due to Incorrect Labeling
FDA ·
FDA Recalls
Encore Medical, LP Recalls Reverse Shoulder Prosthesis (RSP) Humeral Socket Inserts Due to Labeling Error
FDA ·
FDA Recalls
Encore Medical Recalls EMPOWR 3D KNEE Implants Due to Incorrect Labeling
FDA ·
FDA Recalls high
H & N Group Inc. Recalls Frozen Cooked Shrimp Due to Potential Cesium-137 Contamination
FDA ·
FDA Recalls
Hitachi Recalls PROBEAT-CR Proton Beam Therapy System Due to Software Anomaly
FDA ·
FDA Recalls
Immunotech A.S. Issues Recall for Estrone RIA Kits Over Inaccurate Test Results
FDA ·
FDA Recalls
Integra LifeSciences Recalls MEDIHONEY Calcium Alginate Dressings Due to Potential Sterility Breach
FDA ·
FDA Recalls high
Integra LifeSciences Recalls MediHoney Gel Due to Potential Sterile Barrier Breach
FDA ·
FDA Recalls
Integra LifeSciences Recalls Private Label CVS Wound Care Products Over Sterility Concerns
FDA ·
FDA Recalls
Intuitive Surgical Recalls Da Vinci 5 Surgical Consoles Due to Software Error
FDA ·
FDA Recalls high
LEO Pharma Inc. Recalls Adbry Injection Due to Potential Wool Fiber Contamination
FDA ·
FDA Recalls high
Lotus Mom Corporation Recalls Brass Tope Over Potential Lead Contamination
FDA ·
FDA Recalls
Lubna Quality Products Inc. Recalls Mung Beans in Texas and Louisiana Due to Pesticide
FDA ·
FDA Recalls high
Medica Corporation Recalls Capillary Tube Kits Due to Inaccurate Potassium Results
FDA ·
FDA Recalls
Medline Industries Recalls 154,427 Convenience Kits Over Sterility Concerns
FDA ·
FDA Recalls high
Medline Industries Recalls 3,561 Medical Convenience Kits Over Sterility Concerns
FDA ·
FDA Recalls high
Medline Industries Recalls 30,958 Convenience Kits Over Sterility Concerns
FDA ·
FDA Recalls
Medline Industries Recalls 4,853 Convenience Kits Over Sterilization Calibration Issues
FDA ·
FDA Recalls
Medline Industries Recalls 5,346 Medical Convenience Kits Over Sterility Concerns
FDA ·
FDA Recalls
Medline Industries Recalls 7,494 Neuro Convenience Kits Over Sterility Concerns
FDA ·
FDA Recalls high
Medline Industries Recalls 82,597 Surgical Convenience Kits Over Sterility Concerns
FDA ·
FDA Recalls high
Medline Industries Recalls 9,051 Convenience Kits Over Sterility Assurance Concerns
FDA ·
FDA Recalls high
Medline Industries Recalls Admit Kits Due to Potential Sterility Compromise
FDA ·
FDA Recalls
Medline Industries Recalls Arthroscopy Kits and Trays Due to Sterility Concerns
FDA ·
FDA Recalls high
Medline Industries Recalls Basic Nerve Block Trays Due to Sterilization Calibration Issues
FDA ·
FDA Recalls high
Medline Industries Recalls Burn Packs Over Sterilization Equipment Calibration Issues
FDA ·
FDA Recalls high
Medline Industries Recalls C-Section Convenience Kits Due to Sterility Assurance Concerns
FDA ·
FDA Recalls high
Medline Industries Recalls Chest/Breast Convenience Kits Due to Sterility Concerns
FDA ·
FDA Recalls
Medline Industries Recalls Convenience Kits Due to Potential Sterility Assurance Issues
FDA ·
FDA Recalls
Medline Industries Recalls Convenience Kits Due to Potential Sterility Concerns
FDA ·
FDA Recalls
Medline Industries Recalls Convenience Kits Over Potential Sterility Assurance Issues
FDA ·
FDA Recalls
Medline Industries Recalls Convenience Kits Over Potential Sterility Concerns
FDA ·
FDA Recalls
Medline Industries Recalls Convenience Kits Over Sterility Concerns
FDA ·
FDA Recalls high
Medline Industries Recalls Dental Packs Due to Potential Sterility Issues
FDA ·
FDA Recalls high
Medline Industries Recalls Dialysis Dressing Change Kits Due to Tego Connector Seal Defects
FDA ·
FDA Recalls high
Medline Industries Recalls Dialysis On/Off Kits Due to Tego Connector Seal Issues
FDA ·
FDA Recalls high
Medline Industries Recalls Drape Pack-Choice Convenience Kits Over Sterility Concerns
FDA ·
FDA Recalls
Medline Industries Recalls General Closure Convenience Kits Over Sterility Assurance Concerns
FDA ·
FDA Recalls high
Medline Industries Recalls IR Packs and Dialysis Insertion Kits Due to Faulty Tego Connectors
FDA ·
FDA Recalls
Medline Industries Recalls Lithotomy Packs Due to Potential Sterility Concerns
FDA ·
FDA Recalls high
Medline Industries Recalls LVAD Driveline and Central Line Dressing Trays Over Sterility Concerns
FDA ·
FDA Recalls high
Medline Industries Recalls Medical Kits Containing Tego Connectors Due to Seal Defects
FDA ·
FDA Recalls
Medline Industries Recalls Meijer Sterile Saline Wound Wash Over Sterility Concerns
FDA ·
FDA Recalls
Medline Industries Recalls Nail Kits Due to Potential Sterility Concerns
FDA ·
FDA Recalls
Medline Industries Recalls Nail Kits Due to Potential Sterility Issues in Wound Wash
FDA ·
FDA Recalls high
Medline Industries Recalls Over 10,000 Convenience Kits Due to Sterility Concerns
FDA ·
FDA Recalls
Medline Industries Recalls Over 117,000 Convenience Kits Due to Sterility Concerns
FDA ·
FDA Recalls high
Medline Industries Recalls Over 12,000 Surgical Convenience Kits Due to Sterility Concerns
FDA ·
FDA Recalls high
Medline Industries Recalls Over 14,000 Dialysis Kits and Trays Due to Tego Connector Seal Defects
FDA ·
FDA Recalls
Medline Industries Recalls Over 14 Million Surgical Drapes Due to Sterility Concerns
FDA ·
FDA Recalls
Medline Industries Recalls Over 193,000 Surgical Packs Due to Sterilization Concerns
FDA ·
FDA Recalls
Medline Industries Recalls Over 27,000 Convenience Kits Due to Sterility Concerns
FDA ·
FDA Recalls
Medline Industries Recalls Over 39,000 Convenience Kits Due to Sterility Concerns
FDA ·
FDA Recalls high
Medline Industries Recalls Over 4,700 Convenience Kits Due to Sterility Concerns
FDA ·
FDA Recalls
Medline Industries Recalls Over 70 Million Surgical Gowns Due to Sterility Concerns
FDA ·
FDA Recalls high
Medline Industries Recalls Over 926,000 IV Administration and Extension Sets Due to Connector Failure
FDA ·
FDA Recalls
Medline Industries Recalls PPE Kits Due to Potential Sterility Issues
FDA ·
FDA Recalls
Medline Industries Recalls Surgical and Medical Convenience Kits Over Sterility Concerns
FDA ·
FDA Recalls
Medline Industries Recalls Surgical Convenience Kits Over Sterility Concerns
FDA ·
FDA Recalls high
Medline Industries Recalls Tracheostomy Convenience Kits Due to Sterility Concerns
FDA ·
FDA Recalls
Medline Industries Recalls Urology Convenience Kits Over Sterility Assurance Concerns
FDA ·
FDA Recalls
Medline Recalls Convenience GI Kits Over Potential Sterility Assurance Issues
FDA ·
FDA Recalls
Medline Recalls Over 3.5 Million Units of Sterile Saline Wound Wash Due to Sterility Concerns
FDA ·
FDA Recalls high
Medline Recalls Triple Lumen Insertion Kits Over Sterilization Equipment Calibration Issues
FDA ·
FDA Recalls
Medtronic Recalls Octopus Nuvo Tissue Stabilizers Due to Assembly Error
FDA ·
FDA Recalls high
MIN JIANG FOOD STORE INC Recalls Frozen Fish Balls Due to Undeclared Wheat and Sesame
FDA ·
FDA Recalls high
MRIMed Inc. Recalls MRI LED Mobile Exam Light Batteries Due to Overheating and Smoke Hazard
FDA ·
FDA Recalls high
Navitas Organics Recalls Organic Chia Seeds Due to Potential Salmonella Contamination
FDA ·
FDA Recalls
Olympus Corporation of the Americas Recalls Inner Sheath Devices Due to Breaking Ceramic Tips
FDA ·
FDA Recalls
Olympus Corporation Recalls Cystoscope Outer Sheaths Due to Laser Incompatibility
FDA ·
FDA Recalls
Olympus Corporation Recalls Resection Inner Sheaths Due to Ceramic Tip Breakage Risk
FDA ·
FDA Recalls
Olympus Corporation Recalls Resection Sheaths Due to Risk of Ceramic Tip Breakage
FDA ·
FDA Recalls
Olympus Corporation Recalls Resection Sheaths Due to Risk of Ceramic Tip Breaking
FDA ·
FDA Recalls high
Olympus Corporation Recalls Thunderbeat Surgical Devices Due to Adverse Event Reports
FDA ·
FDA Recalls high
Olympus Issues Recall for Inner Sheath Used in Urological Procedures Due to Breaking Ceramic Tips
FDA ·
FDA Recalls
Olympus Issues Recall for Resection Sheath Due to Risk of Ceramic Tip Breakage
FDA ·
FDA Recalls
Olympus Issues Recall for Resection Sheaths Due to Risk of Ceramic Tip Breakage
FDA ·
FDA Recalls high
Olympus Recalls High Flow Insufflation Units Due to Overpressure Risk
FDA ·
FDA Recalls high
Olympus Recalls High Flow Insufflation Units Due to Software-Related Overpressure Risk
FDA ·
FDA Recalls high
Olympus Recalls High Flow Insufflation Units Over Software-Related Overpressure Risk
FDA ·
FDA Recalls
Olympus Recalls Inner Sheath 21 Fr. Model A2660T Over Ceramic Tip Breakage Concerns
FDA ·
FDA Recalls high
Olympus Recalls Inner Sheath Model A2642 Over Reports of Breaking Ceramic Tips
FDA ·
FDA Recalls high
Olympus Recalls Inner Sheaths Due to Risk of Ceramic Tip Breakage
FDA ·
FDA Recalls high
Olympus Recalls Inner Sheaths Used in Gynecological Procedures Due to Breaking Ceramic Tips
FDA ·
FDA Recalls
Olympus Recalls Inner Sheaths Used in Urological and Gynecological Procedures Due to Breakage Risk
FDA ·
FDA Recalls
Olympus Recalls Resection Inner Sheaths Due to Ceramic Tip Breakage
FDA ·
FDA Recalls
Olympus Recalls Resection Sheaths Due to Risk of Ceramic Tip Breakage
FDA ·
FDA Recalls
Olympus Recalls Resection Sheaths Over Ceramic Tip Breakage Risk
FDA ·
FDA Recalls
Olympus Recalls Resection Sheaths Over Risk of Ceramic Tip Breakage
FDA ·
FDA Recalls high
Olympus Recalls Thunderbeat Surgical Devices Due to Adverse Event Reports
FDA ·
FDA Recalls high
Olympus Recalls Thunderbeat Surgical Devices Following Reports of Adverse Events
FDA ·
FDA Recalls high
Oregon Potato Company Recalls IQF Blueberries Due to Listeria monocytogenes Risk
FDA ·
FDA Recalls high
Prime Food Processing LLC Recalls Dried Croaker Fish Due to Uneviscerated Fish Hazard
FDA ·
FDA Recalls high
Pure Solutions, Inc. Recalls Sleep Supplements Due to Undeclared Milk Allergen
FDA ·
FDA Recalls
Remel, Inc. Issues Recall for Campy CVA Medium Over Bacterial Recovery Concerns
FDA ·
FDA Recalls high
Reser's Fine Foods Recalls Molly Kitchen's Tuna Salad Due to Undeclared Fish Allergen
FDA ·
FDA Recalls
SB FOOD LLC Recalls Yoyo Gummy Assorted Flavor Over Unallowed Color Additive
FDA ·
FDA Recalls
SB FOOD LLC Recalls Yoyo Gummy Grape Plus Flavor Over Unallowed Color Additive
FDA ·
FDA Recalls
SB FOOD LLC Recalls Yoyo Gummy Tropical Flavor Over Unapproved Color Additive
FDA ·
FDA Recalls
Slate Run Pharmaceuticals Recalls Eptifibatide Injection Due to Labeling Error
FDA ·
FDA Recalls
Stryker Corporation Recalls MOLLI 2 System Components Over Marker Dislodgement Risk
FDA ·
FDA Recalls
Tengen USA Trading Corp Recalls YO!MAN Cucumber Due to Undeclared Cyclamates
FDA ·
FDA Recalls
Tengen USA Trading Corp Recalls YO!MAN Lettuce Due to Undeclared Cyclamates
FDA ·
FDA Recalls
Valley Springs Artesian Gold Recalls Bottled Water Due to Insanitary Conditions
FDA ·
FDA Recalls
Valley Springs Artesian Gold Recalls Bottled Water Over Insanitary Conditions
FDA ·
FDA Recalls
Valley Springs Steamed Distilled Water Recall Issued Due to Insanitary Bottling Conditions
FDA ·
FDA Recalls high
Vista Gel Hypromellose Eye Drops Recalled Nationwide Due to Sterility Concerns
FDA ·
FDA Recalls high
Vista Gonio Eye Lubricant Recall Issued Due to Sterility Concerns
FDA ·
FDA Recalls high
Vista Meibo Tears Eye Drops Recalled Nationwide Due to Sterility Concerns
FDA ·
FDA Recalls high
Wellsley Farms Farm-Raised Atlantic Salmon Recalled Due to Listeria Risk
FDA ·
FDA Recalls high
Why Not Natural Moringa Capsules Recalled Due to Potential Salmonella Contamination
FDA ·
FDA Recalls high
Wilson-Cook Medical Inc. Recalls Teslatome Bipolar Sphincterotomes Due to Electrical Hazard
FDA ·
FDA Recalls high
Wizcure Pharmaa Recalls Bio Glo Fluorescein Sodium Ophthalmic Strips Due to Sterility Concerns
FDA ·
FDA Recalls
Wizcure Pharmaa Recalls Fluorescein Sodium Ophthalmic Strips Over Sterility Concerns
FDA ·
FDA Recalls
Wizcure Pharmaa Recalls Vista Tears Eye Drops Nationwide Over Sterility Concerns
FDA ·
FDA Recalls
Woodland Foods LLC Recalls Woodland Gourmet Arrowroot Flour Due to Foreign Material
FDA ·
FDA Recalls high
Vortex Surgical Inc. Recalls Disposable Forceps and Cannulas Due to Potential Sterility Breach
FDA ·
FDA Recalls high
Vortex Surgical Inc. Recalls Oertli Laser Probes Due to Potential Sterility Breach
FDA ·
FDA Recalls high
Vortex Surgical Inc. Recalls Tecfen Retractable Membrane Polisher Due to Sterility Concerns
FDA ·
FDA Recalls high
Vortex Surgical Recalls 25GA I.D.D. Internal Delivery Devices Over Sterility Risks
FDA ·
FDA Recalls high
Vortex Surgical Recalls 25GA Subretinal Injection Cannula Due to Potential Sterility Breach
FDA ·
FDA Recalls
Vortex Surgical Recalls Backflush Devices Due to Potential Sterile Barrier Breach
FDA ·
FDA Recalls high
Vortex Surgical Recalls I2 Injection Kits Over Potential Sterility Breach
FDA ·
FDA Recalls high
Vortex Surgical Recalls Laser Probes Due to Potential Sterile Barrier Breach
FDA ·
FDA Recalls
Vortex Surgical Recalls Lindsell Sutured IOL Markers Over Sterility Concerns
FDA ·
FDA Recalls high
Vortex Surgical Recalls Rumex Disposable Diamond Dusted ILM Elevator Over Sterility Concerns
FDA ·
FDA Recalls
Vortex Surgical Recalls TID Pharos Illuminated Depressor Over Potential Safety Issues
FDA ·
FDA Recalls high
Vortex Surgical Recalls Volk Single Use Vitrectomy Lenses Due to Potential Sterility Breach
FDA ·
FDA Recalls
Weaver's Brew LLC Recalls Goldenroot Ginger Beer Over Pasteurization Concerns
FDA ·
FDA Recalls
Weaver's Brew LLC Recalls Goldenroot Lemon Double Ginger Beer Due to Pasteurization Issue
FDA ·
FDA Recalls
Weaver's Brew LLC Recalls Goldenroot Lemon Ginger Elderberry Ginger Beer Over Pasteurization Concerns
FDA ·
FDA Recalls
Willy Pete's Chocolate Company LLC Recalls Almond Despair Chocolates Due to Labeling Error
FDA ·
FDA Recalls
Wilson-Cook Medical Inc. Recalls Nasal Jejunal Feeding Tubes Due to Missing Components
FDA ·
FDA Recalls high
WinCo Foods Recalls Deli Margherita Pizza Due to Potential Metal Fragments
FDA ·
FDA Recalls
Alphatec Spine Recalls ATEC Lateral Navigation Disc Prep Instruments Due to Design Flaw
FDA ·
FDA Recalls
American Health Packaging Recalls Oxycodone Hydrochloride Tablets Due to Defective Blister Seals
FDA ·
FDA Recalls high
Asteria Health Issues Nationwide Recall of Estradiol Sterile Pellets Due to Metal Contamination Concerns
FDA ·
FDA Recalls high
Asteria Health Issues Nationwide Recall of Testosterone Sterile Pellets Due to Metal Particulates
FDA ·
FDA Recalls high
Asteria Health Recalls Estradiol 15 mg Sterile Pellets Due to Potential Metal Contamination
FDA ·
FDA Recalls high
Asteria Health Recalls Estradiol Sterile Pellets Due to Potential Metal Contamination
FDA ·
FDA Recalls
Asteria Health Recalls Estradiol Sterile Pellets Due to Potential Metal Particulate Matter
FDA ·
FDA Recalls high
Asteria Health Recalls Testosterone and Anastrozole Sterile Pellets Due to Metal Particulate Matter
FDA ·
FDA Recalls high
Asteria Health Recalls Testosterone and Anastrozole Sterile Pellets Due to Potential Metal Contamination
FDA ·
FDA Recalls
Asteria Health Recalls Testosterone and Triamcinolone Acetonide Pellets Due to Potential Metal Contamination
FDA ·
FDA Recalls high
Asteria Health Recalls Testosterone Sterile Pellets Due to Potential Metal Contamination
FDA ·
FDA Recalls high
Asteria Health Recalls Testosterone Sterile Pellets Due to Potential Metal Particulate Matter
FDA ·
FDA Recalls
AVID Medical, Inc. Recalls Halyard TRANSPORT BAG KIT Over Potential Sterility Compromise
FDA ·
FDA Recalls high
B.C. Williams Bakery Service, Inc. Recalls Bread and Roll Mix Due to Undeclared Milk Allergen
FDA ·
FDA Recalls high
B.C. Williams Bakery Service Recalls Spice Cake Mix Due to Undeclared Milk Allergen
FDA ·
FDA Recalls high
B.C. Williams Bakery Service Recalls Swiss Chocolate Cake Mix Due to Undeclared Milk Allergen
FDA ·
FDA Recalls
Baxter Healthcare Recalls Sterile Water for Irrigation Due to Plastic Particulate Matter
FDA ·
FDA Recalls high
Beacon Promotions Inc Recalls Repackaged M&Ms Due to Undeclared Milk, Soy, and Peanut Allergens
FDA ·
FDA Recalls high
Beacon Promotions Inc Recalls Repackaged M&Ms Peanut Candies Due to Undeclared Allergens
FDA ·
FDA Recalls
Beckman Coulter Recalls CellMek SPS Sample Preparation System Due to Software Error
FDA ·
FDA Recalls
Beckman Coulter Recalls COULTER DxH Diluent Lots Due to Elevated Platelet Background Counts
FDA ·
FDA Recalls high
Bharat Bazar Recalls Soma Kitchen Natural Asafoetida Due to Undeclared Wheat
FDA ·
FDA Recalls
Biomerieux Inc Recalls VITEK 2 Gram-negative Susceptibility Cards Due to Potential for False Test Results
FDA ·
FDA Recalls high
Boston Scientific Recalls AXIOS Stent and Delivery System Due to Deployment Risks
FDA ·
FDA Recalls high
Boston Scientific Recalls AXIOS Stent and Delivery System Over Deployment Failures
FDA ·
FDA Recalls high
Boston Scientific Recalls AXIOS Stent and Delivery Systems Over Deployment Failures
FDA ·
FDA Recalls high
Boston Scientific Recalls HOT AXIOS Stent and Delivery System Due to Deployment Failures
FDA ·
FDA Recalls high
Boston Scientific Recalls HOT AXIOS Stent and Delivery System Over Deployment Failures
FDA ·
FDA Recalls high
Boston Scientific Recalls HOT AXIOS Stent Systems Due to Deployment and Expansion Issues
FDA ·
FDA Recalls high
Cacao Art Recalls Crunchy Caramel Dark Chocolate Over Undeclared Milk Allergen
FDA ·
FDA Recalls high
Carrot Top Kitchens Issues Recall for Cherry Pepper Hummus Due to Undeclared Sesame
FDA ·
FDA Recalls high
Carrot Top Kitchens Recalls Lemon & Garlic Hummus Over Undeclared Sesame
FDA ·
FDA Recalls high
Carrot Top Kitchens Recalls Lime Ginger Hummus Over Undeclared Sesame Allergen
FDA ·
FDA Recalls high
Carrot Top Kitchens Recalls Sundried Tomato and Caper Hummus Due to Undeclared Sesame
FDA ·
FDA Recalls high
Carrot Top Kitchens Recalls White Truffle Hummus Due to Undeclared Sesame Allergen
FDA ·
FDA Recalls high
Changchun Wancheng Bio-Electron Recalls 32,500 Test Strips Over Marketing and Accuracy Concerns
FDA ·
FDA Recalls
Changchun Wancheng Bio-Electron Recalls LH One Step Ovulation Test Devices Over Lack of FDA Clearance
FDA ·
FDA Recalls
Changchun Wancheng Bio-Electron Recalls Male Fertility Sperm Tests Due to Lack of FDA Clearance
FDA ·
FDA Recalls
Changchun Wancheng Bio-Electron Recalls Menopause Test Cassettes Over Regulatory Concerns
FDA ·
FDA Recalls
Changchun Wancheng Bio-Electron Recalls Over 91,000 UTI and Urinalysis Test Strips Due to Inaccuracy Risk
FDA ·
FDA Recalls
Changchun Wancheng Bio-Electron Recalls S. Typhi/Para Typhi A Antigen Test Strips Over Marketing Concerns
FDA ·
FDA Recalls high
Changchun Wancheng Bio-Electron Recalls Vivoo Protein Test Strips Over Marketing Clearance Issues
FDA ·
FDA Recalls
Changchun Wancheng Bio-Electron Recalls Vivoo Sodium, Vitamin C, and Hydration Tests Due to Marketing Violations
FDA ·
FDA Recalls
Changchun Wancheng Bio-Electron Recalls Vivoo Vaginal pH Tests Due to Lack of Marketing Clearance
FDA ·
FDA Recalls high
Costco Recalls Kirkland Signature Mini Beignets Due to Undeclared Hazelnut
FDA ·
FDA Recalls high
Diva Fam Inc Issues Nationwide Recall of Sea Moss Gel Superfood Over Botulism Concerns
FDA ·
FDA Recalls high
Diva Fam Inc Recalls Mango Sea Moss Gel Superfood Over Potential Botulism Risk
FDA ·
FDA Recalls high
Diva Fam Inc Recalls Sea Moss Gel Superfood Due to Potential Botulism Contamination
FDA ·
FDA Recalls high
Diva Fam Inc Recalls Sea Moss Gel Superfood Due to Potential Botulism Risk
FDA ·
FDA Recalls high
Diva Fam Inc Recalls Sea Moss Gel Superfood Over Potential Botulism Contamination
FDA ·
FDA Recalls high
Elekta, Inc. Recalls Leksell GammaPlan Software Due to Potential Incorrect Patient Irradiation Risk
FDA ·
FDA Recalls high
Elekta, Inc. Recalls Leksell GammaPlan Software Over Radiation Targeting Error
FDA ·
FDA Recalls high
Encore Medical Recalls EMPOWR 3D Knee Tibial Inserts Over Packaging Errors
FDA ·
FDA Recalls
Encore Medical Recalls EMPOWR Acetabular System Liners Due to Packaging Discrepancy
FDA ·
FDA Recalls high
ETAC A/S Recalls Molift 2-Point Sling Bars Due to Structural Bolt Failure Risk
FDA ·
FDA Recalls high
ETAC A/S Recalls Molift 4-Point Sling Bars Due to Risk of Structural Failure
FDA ·
FDA Recalls high
ETAC A/S Recalls Molift Mover 205 Patient Lifts Due to Structural Bolt Failure
FDA ·
FDA Recalls high
ETAC A/S Recalls Molift Mover 300 Mobile Hoists Due to Structural Component Failure
FDA ·
FDA Recalls high
Everpress Juice Issues Recall for 'JUICE from the Raw' Cashew Milk Over Bacterial Concerns
FDA ·
FDA Recalls high
Everpress Juice Issues Recall for 'JUICE from the Raw' Pineapple Mint Over Pathogen Concerns
FDA ·
FDA Recalls high
Everpress Juice Issues Recall for 'JUICE from the Raw' Spicy Lemonade Over Pathogen Risk
FDA ·
FDA Recalls high
Everpress Juice Recalls 'JUICE from the Raw' Cashew Coffee Milk Over Bacterial Concerns
FDA ·
FDA Recalls high
Everpress Juice Recalls 'JUICE from the Raw, DETOX GREENS' Due to Potential Pathogenic Bacteria
FDA ·
FDA Recalls high
Everpress Juice Recalls 'JUICE from the Raw' Sweet Greens Due to Potential Pathogenic Bacteria
FDA ·
FDA Recalls high
Everpress Juice Recalls 'JUICE from the Raw, upbeat' Due to Potential Pathogenic Bacteria
FDA ·
FDA Recalls
Exploro Male Fertility and Sperm Concentration Tests Recalled Due to Lack of FDA Clearance
FDA ·
FDA Recalls high
Focalyx Technologies Recalls Focalyx Fusion Software Due to Windows 10 Compatibility Risks
FDA ·
FDA Recalls high
Fresenius Kabi Compounding, LLC Recalls Thiamine HCl Injection Due to Lack of Sterility Assurance
FDA ·
FDA Recalls high
Fresenius Kabi Compounding Recalls Acyclovir Sodium Injection Due to Sterility Concerns
FDA ·
FDA Recalls high
Fresenius Kabi Compounding Recalls Ketamine HCl Injection Over Sterility Concerns
FDA ·
FDA Recalls high
Fresenius Kabi Compounding Recalls Vancomycin HCl Injection Due to Sterility Concerns
FDA ·
FDA Recalls
FUJIFILM Healthcare Recalls FDR Visionary Suite X-ray Systems Over Overheating and Smoke Risk
FDA ·
FDA Recalls
Fujirebio Diagnostics Recalls Lumipulse β-Amyloid Plasma Controls Over Inaccurate Alzheimer's Test Results
FDA ·
FDA Recalls
Fujirebio Diagnostics Recalls Lumipulse G β-Amyloid 1-42-N Plasma Test Cartridges for Inaccurate Results
FDA ·
FDA Recalls
Fujirebio Diagnostics Recalls Lumipulse G Beta-Amyloid 1-42-N Plasma Calibrators Due to Inaccurate Test Results
FDA ·
FDA Recalls
Fujirebio Diagnostics Recalls Lumipulse G pTau 217 Plasma Calibrators Due to Inaccurate Test Results
FDA ·
FDA Recalls
Fujirebio Diagnostics Recalls Lumipulse G pTau 217 Plasma Immunoreaction Cartridges Due to Inaccurate Results
FDA ·
FDA Recalls
Fujirebio Diagnostics Recalls Lumipulse G pTau217/B-Amyloid 1-42 Plasma Ratio Test Due to Inaccurate Results
FDA ·
FDA Recalls
Fujirebio Diagnostics Recalls Lumipulse pTau 217 Plasma Controls Over Inaccurate Alzheimer's Test Results
FDA ·
FDA Recalls
Goldenroot Lemon Ginger Jalapeno Ginger Beer Recalled Over Pasteurization Concerns
FDA ·
FDA Recalls high
Granules Pharmaceuticals Inc. Recalls Trazodone Hydrochloride Due to Foreign Tablets
FDA ·
FDA Recalls high
Green Lumber Natural Fuel For Men Recall Issued Due to Undeclared Tadalafil
FDA ·
FDA Recalls
Greenstone LLC Recalls Methylprednisolone Dosepak Tablets Due to Dosing Labeling Error
FDA ·
FDA Recalls
Haleon US Holdings LLC Recalls Parodontax Active Gum Health Mouthwash Due to Labeling Issues
FDA ·
FDA Recalls high
Handelnine Global LLC Recalls Rheumacare Capsules Due to Lead Contamination
FDA ·
FDA Recalls high
Hannaford Hamburger Dill Pickle Chips Recalled Due to Potential Glass Contamination
FDA ·
FDA Recalls high
Imu-Tek Animal Health Recalls Immuno-5 Colostrum Powder Due to Undeclared Milk Allergen
FDA ·
FDA Recalls high
Intuitive Surgical Recalls da Vinci 5 Surgeon Console Viewer Displays Over Visualization Risks
FDA ·
FDA Recalls high
Intuitive Surgical Recalls da Vinci X, Xi, and 5 Surgical Systems Due to Software Error
FDA ·
FDA Recalls high
Island Crab Corporation Recalls Smoked Grouper Dip Over Undeclared Allergens
FDA ·
FDA Recalls high
Karison Foods & Snacks, Inc. Recalls ALSI PINNI Due to Undeclared Milk Allergen
FDA ·
FDA Recalls high
Karison Foods & Snacks Recalls Besan Laddoo Due to Undeclared Milk
FDA ·
FDA Recalls high
Karison Foods & Snacks Recalls Panjiri Due to Undeclared Milk Allergen
FDA ·
FDA Recalls
Karison Foods & Snacks Recalls Punjabi Pinni Due to Undeclared Milk Allergen
FDA ·
FDA Recalls
Keurig Dr Pepper Recalls McCafe Decaf K-Cup Pods Due to Potential Caffeine Content
FDA ·
FDA Recalls high
Khee Trading Inc. Recalls Frozen Half Shell Oysters Due to Potential Norovirus Contamination
FDA ·
FDA Recalls
KPCM New York Inc. Recalls Preema Food Colour Powder Over Banned and Undeclared Additives
FDA ·
FDA Recalls
Laerdal Medical Corporation Recalls Compact Suction Unit 4 Due to Electromagnetic Noise Interference
FDA ·
FDA Recalls
Lost and Found Energy Sour Gummy Bear Recall Due to Incorrect Caffeine Labeling
FDA ·
FDA Recalls
Maquet Cardiopulmonary Gmbh Recalls Bubble Sensors Over Cable Durability Concerns
FDA ·
FDA Recalls high
McCain Foods USA Inc Recalls Ore-Ida Tater Tots Due to Plastic Fragments
FDA ·
FDA Recalls
McCain Foods USA Inc. Recalls Sonic Tots Due to Potential Plastic Contamination
FDA ·
FDA Recalls high
Medline Industries Recalls 14 Fr Suction Catheter Kits Due to Incorrect Component Sizing
FDA ·
FDA Recalls
Medline Industries Recalls Adult Catheter Securement Dressing Kits Due to Packaging Defect
FDA ·
FDA Recalls high
Medline Industries Recalls Adult Intubation Trays Over Life-Threatening Catheter Size Error
FDA ·
FDA Recalls
Medline Industries Recalls Anesthesia Artline Packs Due to Potential Packaging Defect
FDA ·
FDA Recalls
Medline Industries Recalls Blood Culture Kits Over Potential Packaging Seal Breach
FDA ·
FDA Recalls
Medline Industries Recalls Medical Convenience Kits Due to BD ChloraPrep Packaging Defect
FDA ·
FDA Recalls
Medline Industries Recalls Medical Convenience Kits Due to Compromised Packaging Seals
FDA ·
FDA Recalls
Medline Industries Recalls Mercy Circumcision Trays Due to Compromised Packaging
FDA ·
FDA Recalls
Medline Industries Recalls Over 21,000 Medical Kits Due to Compromised Swabstick Packaging
FDA ·
FDA Recalls
Medline Industries Recalls Pediatric Catheter Securement Dressing Kits Over Sterility Concerns
FDA ·
FDA Recalls high
Medline Industries Recalls Reprocessed Abbott Inquiry Steerable Diagnostic Catheters Due to Potential Contamination
FDA ·
FDA Recalls high
Medline Industries Recalls Reprocessed Biosense Webster Ultrasound Catheters Due to Potential Contamination
FDA ·
FDA Recalls high
Medline Industries Recalls Reprocessed Livewire Steerable Electrophysiology Catheters Due to Contamination Risk
FDA ·
FDA Recalls high
Medline Industries Recalls Reprocessed Siemens ACUSON AcuNav Ultrasound Catheters Due to Contamination Risk
FDA ·
FDA Recalls high
Medline Industries Recalls Reprocessed St. Jude Diagnostic Electrophysiology Catheters Due to Contamination Risk
FDA ·
FDA Recalls high
Medline Industries Recalls Reprocessed ViewFlex Xtra ICE Catheters Due to Potential Particle Contamination
FDA ·
FDA Recalls high
Medline Industries Recalls Reprocessed Webster CS Catheters Due to Potential Residual Material
FDA ·
FDA Recalls
Medline Industries Recalls Sterile Resuture Packs Due to Potential Packaging Seal Defect
FDA ·
FDA Recalls
Medline Recalls Suture Removal Trays Due to Potential Compromise of Sterile Packaging
FDA ·
FDA Recalls high
Medtronic Recalls MiniMed 780G Insulin Pumps Due to Software Error Suspending Insulin Delivery
FDA ·
FDA Recalls
MG Foods Recalls Spicy Breakfast Burritos Due to Potential Plastic Fragments
FDA ·
FDA Recalls
New Way Import Inc. Recalls Preserved Mustard Over Undeclared Wheat Allergen
FDA ·
FDA Recalls
Novadoz Pharmaceuticals LLC Recalls Glycopyrrolate Oral Solution Due to Impurity Specifications
FDA ·
FDA Recalls
Olympus Corporation Recalls Disposable Triple Lumen Sphincterotomes Due to Potential Device Deformation
FDA ·
FDA Recalls
Olympus Corporation Recalls Disposable Triple Lumen Sphincterotomes Over Performance Concerns
FDA ·
FDA Recalls
Olympus Corporation Recalls Single Use 3-Lumen Sphincterotome V Due to Potential Performance Loss
FDA ·
FDA Recalls
Olympus Recalls CleverCut Single Use 3-Lumen Sphincterotome V Over Performance Concerns
FDA ·
FDA Recalls
Olympus Recalls Disposable Triple Lumen Sphincterotome Due to Potential Deformation and Performance Loss
FDA ·
FDA Recalls
Olympus Recalls Disposable Triple Lumen Sphincterotome Due to Potential Device Deformation
FDA ·
FDA Recalls
Olympus Recalls Disposable Triple Lumen Sphincterotomes Due to Potential Performance Loss
FDA ·
FDA Recalls
Olympus Recalls Single Use 3-Lumen Sphincterotome V Due to Device Deformation Risk
FDA ·
FDA Recalls
Olympus Recalls Single Use 3-Lumen Sphincterotome V Due to Potential Device Deformation
FDA ·
FDA Recalls
Olympus Recalls Single Use 3-Lumen Sphincterotome V Due to Potential Performance Loss
FDA ·
FDA Recalls
Olympus Recalls Single Use 3-Lumen Sphincterotome V Over Performance Concerns
FDA ·
FDA Recalls
Olympus Recalls Single Use Electrosurgical Knife KD-640L Due to Tip Breakage Risk
FDA ·
FDA Recalls high
Olympus Recalls Single Use Electrosurgical Knife KD-645 Over Tip Breakage Concerns
FDA ·
FDA Recalls
Olympus Recalls Single Use Sphincterotome V Due to Potential Performance Failure
FDA ·
FDA Recalls
Optiwize Inc. Issues Voluntary Recall for OptiWize Collagen Plus Over Ingredient Discrepancy
FDA ·
FDA Recalls
Organic Spices, Inc. Recalls Spicely Organic Celery Salt Due to Mislabeling and Salt Content
FDA ·
FDA Recalls
Organic Spices, Inc. Recalls Spicely Organic Garlic Salt Due to Mislabeling Error
FDA ·
FDA Recalls
Organic Spices, Inc. Recalls Spicely Organic Sumac Due to Mislabeled Salt Content
FDA ·
FDA Recalls high
Outside The Breadbox Bread Crumbs Recalled Over Undeclared Egg and Milk
FDA ·
FDA Recalls
Philips Medical Systems Recalls Azurion 3 M12 Systems Due to Unexpected Table Movement
FDA ·
FDA Recalls
Philips Medical Systems Recalls Azurion 3 M15 Systems Due to Unexpected Table Movement
FDA ·
FDA Recalls
Philips Medical Systems Recalls Azurion 5 M12 Systems Over Unexpected Table Movement Hazard
FDA ·
FDA Recalls
Philips Medical Systems Recalls Azurion 7 B12 Systems Due to Unexpected Table Movement
FDA ·
FDA Recalls
Philips Medical Systems Recalls Azurion 7 B20 Systems Due to Unexpected Table Movement
FDA ·
FDA Recalls high
Philips North America Recalls Brilliance iCT Systems Over Potential Projectile Hazard
FDA ·
FDA Recalls
Philips North America Recalls IQon Spectral CT Systems Due to Loose Fastener Risk
FDA ·
FDA Recalls
Philips North America Recalls Spectral CT 7500 on Rails Over Potential Rotor Part Displacement
FDA ·
FDA Recalls
Philips North America Recalls Spectral CT Systems Due to Potential Rotor Component Displacement
FDA ·
FDA Recalls
Philips Recalls Azurion 5 M20 Systems Due to Unexpected Table Movement Hazard
FDA ·
FDA Recalls
Philips Recalls Azurion 7 M12 Systems Due to Unexpected Table Movement Hazard
FDA ·
FDA Recalls
Philips Recalls Azurion 7 M20 Systems Due to Unexpected Table Movement
FDA ·
FDA Recalls high
Plant Based Innovations Recalls Higher Harvest by H-E-B Strawberry Yogurt Due to Undeclared Almonds
FDA ·
FDA Recalls
Prima Foods International Recalls BarbaCuban 455 Everything Sauce Due to Undeclared Quinine
FDA ·
FDA Recalls
Prima Foods International Recalls BarbaCuban 455 Everything Sauce Over Undeclared Quinine
FDA ·
FDA Recalls
Prima Foods International Recalls BarbaCuban Havana Gold Due to Undeclared Quinine
FDA ·
FDA Recalls
Prima Foods International Recalls BarbaCuban Mojo Marinade Over Undeclared Quinine
FDA ·
FDA Recalls
Prima Foods International Recalls BarbaCuban Ram Air Red Zesty Ketchup Due to Undeclared Quinine
FDA ·
FDA Recalls
Prima Foods International Recalls BarbaCuban White Truffle Sauce Due to Undeclared Quinine
FDA ·
FDA Recalls high
Prima Vera Nueva, Inc. Recalls Black Bean Bonanza Tamales Due to Potential Listeria Contamination
FDA ·
FDA Recalls high
Prima Vera Nueva, Inc. Recalls Butternut Squash Tamales Over Listeria Concerns
FDA ·
FDA Recalls high
Prima Vera Nueva, Inc. Recalls Mushroom, Spinach & Salsa Tamales Due to Potential Listeria Contamination
FDA ·
FDA Recalls high
Prima Vera Nueva, Inc. Recalls Roasted Green Chile & Jack Cheese Tamales Due to Potential Listeria Contamination
FDA ·
FDA Recalls high
Primavera BBQ Chipotle Bean & White Cheddar Tamales Recalled Due to Potential Listeria Contamination
FDA ·
FDA Recalls high
Primavera Black Bean Bonanza Tamales Recalled Due to Potential Listeria Contamination
FDA ·
FDA Recalls high
Primavera Recalls Butternut Squash Tamales Due to Potential Listeria Contamination
FDA ·
FDA Recalls high
Primavera Roasted Green Chile Tamales Recalled Due to Potential Listeria Contamination
FDA ·
FDA Recalls high
Primavera Roasted Pumpkin & White Cheddar Tamales Recalled Due to Potential Listeria Contamination
FDA ·
FDA Recalls
Pro Numb Tattoo Numbing Spray Recalled Due to Manufacturing Deviations
FDA ·
FDA Recalls
Pro Numb Tattoo Numbing Spray Recalled Nationwide Due to Manufacturing Deviations
FDA ·
FDA Recalls
Red Button Movie House Popcorn Recall Issued Over Foreign Material Concerns
FDA ·
FDA Recalls
Sato Pharmaceutical Recalls INON ACE Antacid Tablets Due to Disintegration Failure
FDA ·
FDA Recalls
Siemens Medical Solutions Recalls NAEOTOM Alpha.Prime Software Applications Over Lack of FDA Clearance
FDA ·
FDA Recalls
Siemens Medical Solutions Recalls NAEOTOM Alpha.Pro Software Applications Due to Lack of FDA Clearance
FDA ·
FDA Recalls
Siemens Medical Solutions Recalls NAEOTOM Alpha Software Applications Over Missing FDA Clearance
FDA ·
FDA Recalls
Siemens Medical Solutions Recalls SOMATOM X.ceed Software Applications Over Lack of FDA Clearance
FDA ·
FDA Recalls
Steris Corporation Recalls Barco MNA with HexaVue IP Integration System Due to Configuration Error
FDA ·
FDA Recalls
Straumann USA LLC Recalls WB Impression Post Closed Trays Due to Component Mix-Up
FDA ·
FDA Recalls high
Superfoods, Inc. Recalls Live it Up Super Greens Due to Potential Salmonella Contamination
FDA ·
FDA Recalls
SurePulse Medical Ltd Recalls Surepulse VS Cap Medium Over Incorrect Sizing Label
FDA ·
FDA Recalls
SurePulse Medical Ltd Recalls Surepulse VS Cap Small Due to Labeling Error
FDA ·
FDA Recalls
Surepulse Medical Ltd Recalls VS Cap Extra Large Over Labeling Error
FDA ·
FDA Recalls
Surepulse Medical Ltd Recalls VS Cap Extra Small Due to Incorrect Sizing Labeling
FDA ·
FDA Recalls
Surepulse Medical Ltd Recalls VS Cap Large Due to Incorrect Labeling Sizing Guide
FDA ·
FDA Recalls high
Tai Phat Wholesalers Recalls Sofit Seedless Red Dates Due to Undeclared Sulfites
FDA ·
FDA Recalls high
TKS Co-pack Manufacturing Recalls Aonic Complete Hers Supplement Shots Over Bacterial Contamination Concerns
FDA ·
FDA Recalls high
TKS Co-pack Manufacturing Recalls Aonic Complete His Supplement Due to Potential Bacterial Contamination
FDA ·
FDA Recalls
Tornier, Inc. Recalls Reversed Peripheral Screws Due to Labeling Error
FDA ·
FDA Recalls high
Tradin Organics USA LLC Recalls Organic Black Chia Seeds Over Salmonella Concerns
FDA ·
FDA Recalls
Unichem Pharmaceuticals Issues Nationwide Recall of Doxazosin Mesylate Tablets Due to Incorrect Imprint
FDA ·
FDA Recalls
Vantive US Healthcare Recalls Oxiris Set Dialyzers Due to Chamber Dislodgement Risk
FDA ·
FDA Recalls
Vantive US Healthcare Recalls Primsaflex M100 Set Due to Deaeration Chamber Dislodgement Risk
FDA ·
FDA Recalls high
Vantive US Healthcare Recalls Prismaflex HF1000 Sets Due to Component Dislodgement Risk
FDA ·
FDA Recalls
Vantive US Healthcare Recalls PRISMAFLEX M150 Sets Due to Deaeration Chamber Issues
FDA ·
FDA Recalls
Vantive US Healthcare Recalls Prismaflex ST100 Sets Due to Chamber Dislodgement Risk
FDA ·
FDA Recalls
Vantive US Healthcare Recalls Prismaflex ST150 Sets Due to Chamber Dislodgement Risk
FDA ·
FDA Recalls
Vantive US Healthcare Recalls Prismaflex TPE2000 Sets Due to Component Dislodgement Risk
FDA ·
FDA Recalls
Ventura Foods LLC Recalls Multiple Peanut Butter Brands Due to Potential Plastic Contamination
FDA ·
FDA Recalls
Ventura Foods LLC Recalls Poco Pac Peanut Butter and Jelly Packs Over Plastic Contamination
FDA ·
FDA Recalls
Ventura Foods LLC Recalls Poco Pac Peanut Butter and Strawberry Jam Due to Potential Plastic Contamination
FDA ·
FDA Recalls high
Venzu Traders LLC Recalls Cinnamon Powder Due to Potential Lead Contamination
FDA ·
FDA Recalls
Vivoo pH Test Recalled Due to Lack of Marketing Clearance and Risk of Inaccurate Results
FDA ·
FDA Recalls high
Vortex Surgical Inc. Recalls Convenience Kits Over Potential Sterility Breach
FDA ·
FDA Recalls
Olympus Recalls ShockPulse-SE Lithotripsy System Probes Due to Recognition Issues
FDA ·
FDA Recalls
Advanced Bionics Recalls Sky CI M90 Sound Processors Due to Labeling Error
FDA ·
FDA Recalls
Olympus Recalls ShockPulse-SE Lithotripsy Systems Due to Mis-wired Components
FDA ·
FDA Recalls
Vascutek, Ltd. Recalls Gelsoft Plus and Gelweave Vascular Devices Due to Incorrect Shelf Life Labeling
FDA ·
FDA Recalls
Diagnostica Stago Recalls STA Liatest Free Protein S Kits for Inaccurate Test Results
FDA ·
FDA Recalls
Olympus Recalls ShockPulse-SE Lithotripsy System Reusable Probes Due to Recognition Issues
FDA ·
FDA Recalls
Datascope Corp. Recalls CS100 IABP Devices Due to Battery Specification Updates
FDA ·
FDA Recalls
Siemens Healthcare Diagnostics Recalls Atellica CH Urine Albumin Test Kits Due to Inaccurate Results
FDA ·
FDA Recalls
Datascope Corp. Recalls CS300 IABP Devices to Update Battery Specifications
FDA ·
FDA Recalls high
GE Healthcare Recalls Centricity Universal Viewer Zero Footprint Client Due to Patient Data Mismatch
FDA ·
FDA Recalls high
Roche Diagnostics Recalls cobas pro Integrated Solutions Due to Software Defect
FDA ·
FDA Recalls
ESAOTE S.P.A. Recalls Endocavity Ultrasonic Probes Due to Potential Liquid Leakage
FDA ·
FDA Recalls
Aesculap Inc. Recalls MINOP Trocar Devices Due to Incorrect Shaft Length
FDA ·
FDA Recalls high
Staar Surgical AG Recalls EVO+ Visian Toric Implantable Collamer Lenses Due to Labeling Error
FDA ·
FDA Recalls high
Abiomed Recalls Impella RP Heart Pumps Over Sensor Malfunction Risks
FDA ·
FDA Recalls
Olympus Recalls ShockPulse-SE Lithotripsy System Generators Over Recognition Failure
FDA ·
FDA Recalls high
Abiomed, Inc. Issues Recall for Impella RP with SmartAssist Over Sensor Malfunction
FDA ·
FDA Recalls
Olympus Recalls Single Use Biopsy Valves Due to Rubber Fragment Detachment Risk
FDA ·
FDA Recalls high
Abiomed Recalls Impella RP Flex with SmartAssist Heart Pumps Due to Sensor Malfunction
FDA ·
FDA Recalls high
Olympus Recalls Single Use Biopsy Valves Due to Potential Rubber Fragment Detachment
FDA ·
FDA Recalls
Bader Enterprises, Inc. Recalls Premium Food Bubble Gum Over Undeclared Colors
FDA ·
FDA Recalls
Bader Enterprises Recalls Premium Food Jordan Almonds Over Undeclared Wheat and Colors
FDA ·
FDA Recalls
Italianway Import, Inc. Recalls Vergani 1944 Milano Gluten-Free Pandoro Due to Potential Teflon Contamination
FDA ·
FDA Recalls high
Juniper Granola, LLC Recalls Junebar Snack Bars Due to Undeclared Milk and Soy
FDA ·
FDA Recalls
Tippy Toes Apple Pear Banana Baby Food Recalled Over Patulin Contamination Concerns
FDA ·
FDA Recalls high
Juniper Granola Recalls Junebar Chocolate Cherry Snack Bars Due to Undeclared Milk and Soy
FDA ·
FDA Recalls high
SILINTAN 25/pills Recalled Nationwide Due to Undeclared Meloxicam
FDA ·
FDA Recalls
Acme United Corporation Recalls Children's Healthcare of Atlanta Hand Sanitizing Wipes
FDA ·
FDA Recalls
Acme United Corporation Recalls BZK Antiseptic Towelettes Due to Manufacturing Deviations
FDA ·
FDA Recalls
ACME UNITED CORPORATION Recalls WP WipesPlus Hand Sanitizing Wipes Due to Manufacturing Deviations
FDA ·
FDA Recalls
Acme United Corporation Recalls Green Guard Antiseptic Wipes Due to Manufacturing Deviations
FDA ·
FDA Recalls
Radnostix Recalls Sodium Iodide I-131 Therapeutic Oral Solution Due to Particulate Matter
FDA ·
FDA Recalls
Cipla USA Inc. Issues Nationwide Recall for Nilotinib Capsules Due to Appearance Defects
FDA ·
FDA Recalls
Harbin Jixianglong Biotech Co. Issues Nationwide Recall of Semaglutide Over Manufacturing Deviations
FDA ·
FDA Recalls
Acme United Corporation Recalls Dukal BZK Antiseptic Towelettes Due to CGMP Deviations
FDA ·
FDA Recalls
Medi-First Antiseptic Wipes Recalled Nationwide Due to Manufacturing Deviations
FDA ·
FDA Recalls
ACME UNITED CORPORATION Recalls Max Packaging Antibacterial Towelettes Due to CGMP Deviations
FDA ·
FDA Recalls
ACME UNITED CORPORATION Recalls Antimicrobial Alcohol Hand Wipes Due to CGMP Deviations
FDA ·
FDA Recalls
Teva Pharmaceuticals Recalls Metoprolol Succinate Extended-Release Tablets Due to Dissolution Failure
FDA ·
FDA Recalls
ACME UNITED CORPORATION Recalls Dynarex Obstetrical Towelettes Cleanser Due to CGMP Deviations
FDA ·
FDA Recalls
HTO Nevada Inc. Issues Recall for Maximum Zone 1 Lidocaine Cream Due to Stability Concerns
FDA ·
FDA Recalls
Acme United Corporation Recalls First Aid Only Hand Sanitizing Wipes Due to Manufacturing Deviations
FDA ·
FDA Recalls
Acme United Corporation Recalls Med-Nap BZK Antiseptic Towelettes Due to CGMP Deviations
FDA ·
FDA Recalls
ACME United Corporation Recalls Savannah Antibacterial Towelettes Due to CGMP Deviations
FDA ·
FDA Recalls
Acme United Corporation Recalls Med-Nap Cleansing Towelettes Due to CGMP Deviations
FDA ·
FDA Recalls
HTO Nevada Inc. Recalls Zone 2 Lidocaine Cream Over Stability Concerns
FDA ·
FDA Recalls
HTO Nevada Inc. Issues Nationwide Recall of VASOCAINE Spray Due to Stability Concerns
FDA ·
FDA Recalls
ACME UNITED CORPORATION Recalls Wipes Plus Hand Sanitizing BZK Wipes Due to CGMP Deviations
FDA ·
FDA Recalls
Acme United Corporation Recalls First Aid Only BZK Antiseptic Towelettes Due to CGMP Deviations
FDA ·
FDA Recalls high
Harbin Jixianglong Biotech Recalls Semaglutide for Compounding Due to CGMP Deviations
FDA ·
FDA Recalls
Major Pharmaceuticals Recalls Midodrine Hydrochloride Tablets Over Packaging Defect
FDA ·
FDA Recalls
Acme United Corporation Recalls Dynarex BZK Antiseptic Towelettes Due to Manufacturing Deviations
FDA ·
FDA Recalls
Acme United Corporation Recalls Med Nap Benzalkonium Chloride Antiseptic Towelettes Due to CGMP Deviations
FDA ·
FDA Recalls
Cipla USA Inc. Issues Voluntary Recall for Nilotinib Capsules Due to Stability Test Failure
FDA ·
All federal data sources used on this page
- FDA Enforcement Report - official FDA recall classifications for food, drugs, devices, biologics, and tobacco. fda.gov/safety/recalls
- FDA Recalls, Withdrawals & Safety Alerts API - openFDA recall endpoint. open.fda.gov
- USDA Food Safety and Inspection Service (FSIS) - meat, poultry, and processed-egg-product recalls. fsis.usda.gov/recalls
- CDC Foodborne Outbreaks - outbreak investigation context for food recalls. cdc.gov/foodsafety/outbreaks
- Consumer Product Safety Commission (CPSC) - non-food consumer-product recalls cross-reference. cpsc.gov/recalls
- NHTSA Vehicle Recalls - automobile and tire recalls cross-reference. nhtsa.gov/recalls