FDA Recalls - April 2026 (361 reports)
FDA Recalls issued during April 2026.
April 2026 ran 105% above the trailing 12-month average of 176 reports/month.
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 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
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