FDA Recalls - August 2026 (761 reports)
FDA Recalls issued during August 2026.
August 2026 ran 103% above the trailing 12-month average of 375 reports/month.
FDA Recalls
Quantum 4Front 2HD Wheelchair Recall Issued
FDA ·
FDA Recalls
Quantum Rehab Q6 Edge 2.0 Wheelchair Recall
FDA ·
FDA Recalls
Stryker Strykeflow Suction/Irrigator PS Recall
FDA ·
FDA Recalls
Quantum Rehab Q6 Edge 4 Wheelchair Recall
FDA ·
FDA Recalls
COAPTIUM CONNECT Recall Issued by TISSIUM SA
FDA ·
FDA Recalls
Stryker AHTO Tube Set With Tip Packaging Recall
FDA ·
FDA Recalls
Maquet Flow Anesthesia Machines Recall
FDA ·
FDA Recalls
Philips Allura Xper Systems Recall
FDA ·
FDA Recalls
U2 Total Knee System Femoral Offset Bushing Recall
FDA ·
FDA Recalls
Boston Scientific Radial Jaw 4 Biopsy Forceps Recall
FDA ·
FDA Recalls
COAPTIUM CONNECT Recall Issued by TISSIUM SA
FDA ·
FDA Recalls
Merge OrthoPACS Recall Issued for Display Issue
FDA ·
FDA Recalls
Kingfisher Compact Individual First Aid Kit Recall
FDA ·
FDA Recalls
Aniara Diagnostica Recalls 5-PLASMA Bivalirudin Control
FDA ·
FDA Recalls
COAPTIUM CONNECT Device Recall
FDA ·
FDA Recalls
Aniara Diagnostica Recalls 5-PLASMA Bivalirudin Calibrator
FDA ·
FDA Recalls
Biomet Intramedullary Bone Saw Blade Assembly Recall
FDA ·
FDA Recalls
Quantum Q6 Edge 2.0 Wheelchair Recall
FDA ·
FDA Recalls
Stryker Single Spike Tube Set Recall Issued
FDA ·
FDA Recalls
Siemens Syva Emit Disopyramide Assay Recall
FDA ·
FDA Recalls
Philips Azurion X-Ray Systems Recall for Hard Drive Issue
FDA ·
FDA Recalls
Neuroguard IEP Carotid Stent System Recall
FDA ·
FDA Recalls
GEM Premier 7000 with iQM3 Recall Issued
FDA ·
FDA Recalls high
Halyard Convenience Kits Recall
FDA ·
FDA Recalls
Philips Allura X-Ray System Recall
FDA ·
FDA Recalls
Beckman Coulter MicroScan LabPro V5.03 Recall
FDA ·
FDA Recalls
DASH Rapid PCR Instrument Recall Issued by Nuclein LLC
FDA ·
FDA Recalls
Therabody Theragun Charger Recall Issued
FDA ·
FDA Recalls
REMISOL Advance Software Version 2.5 Recall
FDA ·
FDA Recalls
Quantum Rehab Q6 Edge 3 Wheelchair Recall
FDA ·
FDA Recalls
Quantum Rehab R-TRAK Powered Wheelchair Recall
FDA ·
FDA Recalls
Biomet Recalls Intramedullary Bone Saw Blade Assembly
FDA ·
FDA Recalls
COAPTIUM Connect Device Recall Issued
FDA ·
FDA Recalls
Hardy Diagnostics Recalls HardyDisk AST Cefiderocol (Z-2887-2026)
FDA ·
FDA Recalls
Quantum Rival Wheelchair Recall
FDA ·
FDA Recalls
Quantum Rehab Q6 Edge HD Wheelchair Recall
FDA ·
FDA Recalls
COAPTIUM CONNECT Device Recall by TISSIUM
FDA ·
FDA Recalls
Biofire Defense FilmArray NGDS Warrior Panel Recall
FDA ·
FDA Recalls high
Boston Scientific INFINION CX Lead Kits Recall
FDA ·
FDA Recalls
Quantum 1450 Powered Wheelchair Recall
FDA ·
FDA Recalls
Quantum Rehab 4Front Powered Wheelchair Recall
FDA ·
FDA Recalls
Intramedullary Bone Saw Blade Assembly Recall
FDA ·
FDA Recalls
Merge PACS Medical Imaging Workstation Recall
FDA ·
FDA Recalls
Biomet Intramedullary Bone Saw Blade Assembly Recall
FDA ·
FDA Recalls
U2 Total Knee System Femoral Valgus Offset Adaptor Recall
FDA ·
FDA Recalls
munevo DRIVE Wheelchair Control System Recall
FDA ·
FDA Recalls
Boston Scientific Radial Jaw 4 Biopsy Forceps Recall
FDA ·
FDA Recalls
COAPTIUM CONNECT Device Recall
FDA ·
FDA Recalls
Biomet Intramedullary Bone Saw Blade Assembly Recall
FDA ·
FDA Recalls
Quantum 4Front 2 Wheelchair Recall Issued
FDA ·
FDA Recalls
GE Healthcare Portrait Core Services SW V 1.2.0 Recall
FDA ·
FDA Recalls
Nerivio Infinity Recall Issued for Battery Issue
FDA ·
FDA Recalls high
Halyard Cardiac Cath Pack Recall Due to Particulates
FDA ·
FDA Recalls
Stryker AHTO Tube Set Packaging Recall
FDA ·
FDA Recalls
Innovasis Anti-Torque Instrument Recall
FDA ·
FDA Recalls
USTAR II Knee System Recall Issued
FDA ·
FDA Recalls
Stryker AHTO Dual Spike Tube Set Packaging Recall
FDA ·
FDA Recalls
GEM Premier 5000 PAK Recall Issued by Instrumentation Laboratory
FDA ·
FDA Recalls
COAPTIUM CONNECT Recall Issued for Shelf Life Labeling
FDA ·
FDA Recalls
Aniara Diagnostica Recalls 5-PLASMA Bivalirudin AMR Verification Kit
FDA ·
FDA Recalls
WASPLab Recall Issued Over Software Issue
FDA ·
FDA Recalls
Happiest Baby Pre-loved SNOO Smart Sleeper Recall
FDA ·
FDA Recalls
COAPTIUM CONNECT Recall Issued for Shelf Life Labeling
FDA ·
FDA Recalls
Quantum Outback Powered Wheelchair Recall
FDA ·
FDA Recalls
Quantum Rehab Q6 Edge 3 Stretto Wheelchair Recall
FDA ·
FDA Recalls
U2 Total Knee System PSA Box Trial Recall
FDA ·
FDA Recalls
Boston Scientific Radial Jaw 4 Jumbo Biopsy Forceps Recall
FDA ·
FDA Recalls high
Halyard Convenience Kits Recall Due to Particulates
FDA ·
FDA Recalls
United Orthopedic Corp. Recalls U2 Total Knee System Femoral Offset Bushing
FDA ·
FDA Recalls
Blom-Singer Classic Indwelling Voice Prosthesis Recall Issued
FDA ·
FDA Recalls
Blom-Singer Classic Indwelling Voice Prosthesis Recall
FDA ·
FDA Recalls
Beckman Coulter MicroScan LabPro V5.03 Panel Update Recall
FDA ·
FDA Recalls
GE Healthcare MAC VU360 Electrocardiograph Recall
FDA ·
FDA Recalls
FORWARD Oral Airway Kit Recall Issued by Integrated Medcraft LLC
FDA ·
FDA Recalls
MC2 Portable X-Ray System Recall
FDA ·
FDA Recalls
Siemens Atellica CH Urine Albumin Recall
FDA ·
FDA Recalls
U2 Total Knee System Femoral Valgus Adaptor Recall
FDA ·
FDA Recalls
Siemens Syva Emit tox Serum Tricyclic Antidepressant Calibrator/Controls Recall
FDA ·
FDA Recalls high
Clover Hill Dairy Cheese Recall for Listeria
FDA ·
FDA Recalls
Ultimate Mother's Day Wangshin Doenjang Recall for Undeclared Fish Allergen
FDA ·
FDA Recalls high
La Colonia Foods Recalls Requeson Over Listeria Risk
FDA ·
FDA Recalls high
Clover Hill Dairy Recalls Horseradish Flavored Cheese
FDA ·
FDA Recalls high
La Colonia Foods Recalls Salvadoreno Requeson Soft Ricotta
FDA ·
FDA Recalls high
Clover Hill Dairy Cuajada Recall Over Listeria Contamination
FDA ·
FDA Recalls high
Selectos Latinos Requeson Salvadoreno Cheese Recall
FDA ·
FDA Recalls high
Clover Hill Dairy Mild Cheese Variety Recall
FDA ·
FDA Recalls high
Clover Hill Dairy Smoked Cheddar Cheese Recall
FDA ·
FDA Recalls high
Clover Hill Dairy Soft Cuajada Recall
FDA ·
FDA Recalls
Hondashi 0.25oz Seasoning Recall Due to Undeclared Fish Allergen
FDA ·
FDA Recalls high
Clover Hill Dairy Soft Cuajada Crumbs Recall
FDA ·
FDA Recalls
Eunha Fisheries Recalls Sliced Korean Halibut Over Undeclared Allergens
FDA ·
FDA Recalls high
Clover Hill Dairy Jalapeno Cheddar Cheese Recall
FDA ·
FDA Recalls
Eunha Fisheries Flounder Sashimi Recall for Undeclared Allergens
FDA ·
FDA Recalls
Big Way Hot Pot Miso Paste Recall for Undeclared Milk
FDA ·
FDA Recalls high
Ashfiat Alharamain Energy Support Recall for Undeclared Tadalafil
FDA ·
FDA Recalls high
Clover Hill Dairy Flavored Cheese Recall
FDA ·
FDA Recalls
Cheer Pack Food Pouches Recalled for Plastic Strip Risk
FDA ·
FDA Recalls high
Clover Hill Dairy Fresh Cheddar Curd Recall for Listeria
FDA ·
FDA Recalls high
Clover Hill Dairy Recalls Soft Ricotta Products Due to Listeria
FDA ·
FDA Recalls high
Clover Hill Dairy Pepper Jack Cheese Recall
FDA ·
FDA Recalls high
Clover Hill Dairy Sharp Cheese Snack Pack Recall
FDA ·
FDA Recalls high
Clover Hill Dairy Soft Cuajada in Brine Recall
FDA ·
FDA Recalls
PT Organics Recalls Peter Rabbit Organics Banana & Strawberry Puree
FDA ·
FDA Recalls high
Clover Hill Dairy Pepper Jack Cheese Recall
FDA ·
FDA Recalls high
Clover Hill Dairy Cheese Recall for Listeria
FDA ·
FDA Recalls high
Zen Principle Naturals Moringa Leaf Powder Recall
FDA ·
FDA Recalls high
Clover Hill Dairy Pepper Jack Cheese Recall
FDA ·
FDA Recalls high
M.G. Foods Spicy Breakfast Burrito Recall for Undeclared Soy
FDA ·
FDA Recalls high
Clover Hill Dairy Cheese Recall Due to Listeria
FDA ·
FDA Recalls high
Selectos Latinos Requeson Mexicano Mexican Cottage Cheese Recall
FDA ·
FDA Recalls high
Cyclophosphamide for Injection Recall Due to Particulate Matter
FDA ·
FDA Recalls
Zydus Mirabegron Tablets Recall Due to Impurity
FDA ·
FDA Recalls
Central Admixture Pharmacy Services Recalls Pediatric TPN Bags
FDA ·
FDA Recalls high
Cyclophosphamide for Injection Recall Due to Particulate Matter
FDA ·
FDA Recalls
Dicyclomine Hydrochloride Capsules Recall Issued by Aurobindo
FDA ·
FDA Recalls
GEM Premier 5000 Recall Due to Barcode Reader Issue
FDA ·
FDA Recalls
Argon Medical Devices Recalls L-Cath PICC Catheters
FDA ·
FDA Recalls
Stryker Hoffmann II Connecting Rod Recall
FDA ·
FDA Recalls
Medtronic EOPA Arterial Cannula Recall
FDA ·
FDA Recalls
GEM Premier 5000 and 7000 Recalled Over Barcode Reader Issue
FDA ·
FDA Recalls
AMS ALIGNED MEDICAL SOLUTIONS Kits Recall Issued
FDA ·
FDA Recalls
AMS Angio Pack Recall Issued for Convenience Kits
FDA ·
FDA Recalls
AMS Medical Convenience Kits Recall Due to Lidocaine Quality Issues
FDA ·
FDA Recalls high
Medical Action Industries Angiography Pack Recall
FDA ·
FDA Recalls
Permobil M5 Corpus Power Wheelchair Recall
FDA ·
FDA Recalls
Stryker Hoffmann II Connecting Rod Micro Recall
FDA ·
FDA Recalls
Philips Ingenuity CT Systems Subject to FDA Recall
FDA ·
FDA Recalls
AMS Spinal Kit Recall Issued by Windstone Medical Packaging
FDA ·
FDA Recalls
Stryker Hoffmann II Connecting Rod Micro Recall Issued
FDA ·
FDA Recalls
Stryker Hoffmann II Connecting Rod Micro Recall
FDA ·
FDA Recalls
Philips Brilliance CT Systems Recall Issued by FDA
FDA ·
FDA Recalls
Permobil M3 Corpus Power Wheelchair Recall
FDA ·
FDA Recalls
Medtronic EOPA Arterial Cannula Recall Issued
FDA ·
FDA Recalls
Medtronic EOPA Arterial Cannula Recall for Leak Risk
FDA ·
FDA Recalls
Windstone Medical Packaging Recalls AMS Medical Convenience Kits
FDA ·
FDA Recalls
GEM Premier 7000 with iQM3 Recall
FDA ·
FDA Recalls
Argon Medical L-Cath Midline Catheter Recall
FDA ·
FDA Recalls
Medtronic EOPA 3D Arterial Cannula Recall
FDA ·
FDA Recalls
AMS Aligned Medical Solutions Neuro Packs Recall
FDA ·
FDA Recalls
Medtronic EOPA 3D Arterial Cannula Recall
FDA ·
FDA Recalls
Philips IQon Spectral CT Recall
FDA ·
FDA Recalls
Terex Utilities Power Over Fiber Base Module Recall
FDA ·
FDA Recalls
AMS Block Tray Medical Kits Recall
FDA ·
FDA Recalls
AMS Heart Cath Tray Recall Issued by Windstone Medical Packaging
FDA ·
FDA Recalls
Stryker Hoffmann II Connecting Rod Micro Recall
FDA ·
FDA Recalls
AMS Aligned Medical Solutions Port Tray Kits Recall
FDA ·
FDA Recalls
GEM Premier 5000 Recall Issued for Blood Analyzer Systems
FDA ·
FDA Recalls
IsoTis OrthoBiologics Recalls OsteoBallast Bone Graft Products
FDA ·
FDA Recalls
Windstone Medical Packaging Recalls AMS ENT Packs
FDA ·
FDA Recalls high
ResMed Astral 100/150 Ventilators Recall
FDA ·
FDA Recalls
GEM Premier 5000 Recall
FDA ·
FDA Recalls
Stryker Hoffmann II Connecting Rod Micro Recall
FDA ·
FDA Recalls
Medtronic EOPA Arterial Cannula Recall
FDA ·
FDA Recalls
Stryker Hoffmann II Connecting Rod Micro Recall
FDA ·
FDA Recalls
GEM Premier 5000 Blood Analyzer Recall
FDA ·
FDA Recalls
AMS Aligned Medical Solutions Kits Recall
FDA ·
FDA Recalls
AMS Medical Convenience Kits Recall Due to Lidocaine Quality Issues
FDA ·
FDA Recalls
Mellish Island Super Skin Recall Issued for Undeclared Fish Source
FDA ·
FDA Recalls high
Nelson & Isa Lacteos LLC Recalls Requeson Over Listeria Risk
FDA ·
FDA Recalls
DQ Chocolate Reduced Fat Ice Cream Mix Recall
FDA ·
FDA Recalls
Dorzolamide Hydrochloride and Timolol Maleate Ophthalmic Solution Recall
FDA ·
FDA Recalls
Mycophenolate Mofetil for Injection Recall Due to Precipitate
FDA ·
FDA Recalls
Glenmark Azelaic Acid Gel Recall Due to Texture Complaints
FDA ·
FDA Recalls
Olympus 4K UHD LCD Monitor Recall Issued
FDA ·
FDA Recalls high
Medline Industries LP Recalls Convenience Kits
FDA ·
FDA Recalls
Boston Scientific FARADRIVE STEERABLE SHEATH Recall
FDA ·
FDA Recalls
Boston Scientific FARADRIVE Steerable Sheath Recall
FDA ·
FDA Recalls
Medline NEURO PACK Kits Recall
FDA ·
FDA Recalls
Silent Nite Sleep Appliance Recall Issued
FDA ·
FDA Recalls
3mensio Workstation Software Recall by PIE Medical Imaging
FDA ·
FDA Recalls
SeaSpine Polyaxial Head Recall Issued
FDA ·
FDA Recalls
Boston Scientific Recalls FARADRIVE STEERABLE SHEATH
FDA ·
FDA Recalls
Emano Flow Software Recall Due to Sampling Rate Issue
FDA ·
FDA Recalls
Medline Prostate Robotic Kits Recall
FDA ·
FDA Recalls
Boston Scientific TheraSphere 360 Y-90 Management Platform Recall
FDA ·
FDA Recalls
Medline Convenience Kits Recall Due to Foley Catheters
FDA ·
FDA Recalls
Olympus UHI-4 Insufflation Unit Recall
FDA ·
FDA Recalls high
Medline HIP CDS-LF Procedure Kit Recall
FDA ·
FDA Recalls
Medline Convenience Kits Recall Due to Foley Catheters
FDA ·
FDA Recalls
Medline DAVINCI PROSTATE PACK Kits Recall
FDA ·
FDA Recalls
Medline Convenience Kits Recall for Potential Contamination
FDA ·
FDA Recalls
Medline Convenience Kits Recall Involving Bard Silastic Foley Catheters
FDA ·
FDA Recalls high
Medline C-Section Convenience Kits Recall
FDA ·
FDA Recalls
SnapshotGLO Wound Imaging Device Recall Issued
FDA ·
FDA Recalls
Halyard EYE PACK Recall Issued for Incorrect Betadine Concentration
FDA ·
FDA Recalls
BOSS Xe Family Recall Issued by Wilcox Industries
FDA ·
FDA Recalls
Medline Convenience Kits Recall Due to Catheter Issue
FDA ·
FDA Recalls high
Medline Anterior Hip Kit Recall Issued for Quality Issues
FDA ·
FDA Recalls
Paragon 28 Recalls Phantom Hindfoot Guide Rod (Z-2758-2026)
FDA ·
FDA Recalls
Boston Scientific FARASTAR PFA Generator Recall
FDA ·
FDA Recalls
Medtronic Ventriculostomy Kit Recall Issued
FDA ·
FDA Recalls
Medline Convenience Kits Recall Issued
FDA ·
FDA Recalls
Medline Convenience Kits Recall Due to Foley Catheters
FDA ·
FDA Recalls
Medline Convenience Kits Recall for Potential Contamination
FDA ·
FDA Recalls
Medline Urology Robotic Procedure Pack Recall
FDA ·
FDA Recalls
Ferno-Washington Recalls Power F2 Powered Fastening System
FDA ·
FDA Recalls
Boston Scientific FARASTAR Pulsed Field Ablation Generator Recall
FDA ·
FDA Recalls
Medline Convenience Kits Recall for Bard Silastic Foley Catheters
FDA ·
FDA Recalls
Karl Storz Endoscopy Recalls Flexible Hystero-Fiberscope Kits
FDA ·
FDA Recalls
ICU Medical Hotline Fluid Warming Set Recall
FDA ·
FDA Recalls high
Medline Procedure Kits Recall
FDA ·
FDA Recalls
Boston Scientific FARASTAR Ablation Generator Recall
FDA ·
FDA Recalls
Medtronic MiniMed Go App Recall Due to Missed Alerts
FDA ·
FDA Recalls
Alphatec Spine Recalls SafeOp Patient Interface
FDA ·
FDA Recalls
Penumbra RED 68 Reperfusion Catheter Recall
FDA ·
FDA Recalls
Halyard STANDARD LINE INSERTION PACK Recall
FDA ·
FDA Recalls
Boston Scientific FARASTAR Ablation Generator Recall
FDA ·
FDA Recalls
Boston Scientific Recalls FARADRIVE STEERABLE SHEATH CLEAR
FDA ·
FDA Recalls high
Fusia Asian Inspirations Kimchi & Tofu Kimbap Recall for Undeclared Fish
FDA ·
FDA Recalls
Nautilus Imitation Crab Sticks Recall Due to Undeclared Additive
FDA ·
FDA Recalls high
TNVitamins Moringa Capsules and Powder Recall
FDA ·
FDA Recalls
Island Pacific Imitation Crab Sticks Recall
FDA ·
FDA Recalls
Island Pacific Imitation Crab Flakes Recall
FDA ·
FDA Recalls high
Modern Warrior Ready Dietary Supplement Recall
FDA ·
FDA Recalls
Vintage Roots Root Beer Syrup Recall
FDA ·
FDA Recalls
Man Fon Wonton Wrappers Recall for Undeclared Wheat
FDA ·
FDA Recalls
Man Fon Inc. Won Ton Wrappers Recall for Undeclared Colors
FDA ·
FDA Recalls
Brooklyn Roasting Company Pasteurized Cold Brew Concentrate Recall
FDA ·
FDA Recalls high
Green Jeeva LLC Recalls Organic Moringa Powder
FDA ·
FDA Recalls
Rohto Cooling Eye Drops Dry Aid Recall
FDA ·
FDA Recalls
Major Pharmaceuticals Levothyroxine Sodium Tablets Recall
FDA ·
FDA Recalls
Rohto Cooling Eye Drops ALL-IN-ONE Recall
FDA ·
FDA Recalls
Rising Cyproheptadine Hydrochloride Syrup Recall
FDA ·
FDA Recalls
Levothyroxine Sodium Tablets Recall for Subpotent Drug
FDA ·
FDA Recalls
Levothyroxine Sodium Tablets Recall Issued by Major Pharmaceuticals
FDA ·
FDA Recalls
Glycopyrrolate Injection Recall Due to Particulate Matter
FDA ·
FDA Recalls
Xylocaine Lidocaine HCl Injection Recall for Particulate Matter
FDA ·
FDA Recalls
Rohto Cooling Eye Drops Optic Glow Recall Issued
FDA ·
FDA Recalls
Levothyroxine Sodium Tablets Recall by Major Pharmaceuticals
FDA ·
FDA Recalls
Levothyroxine Sodium Tablets Recall Due to Subpotency
FDA ·
FDA Recalls
Ascend Laboratories Recalls Amlodipine and Olmesartan Medoxomil Tablets
FDA ·
FDA Recalls
Lidolog Kit Recall Issued for Labeling Issue
FDA ·
FDA Recalls
Rohto Cooling Eye Drops Max Strength Recall
FDA ·
FDA Recalls
Fresenius Kabi Lidocaine HCl Injection Recall
FDA ·
FDA Recalls
Major Pharmaceuticals Levothyroxine Sodium Tablets Recall
FDA ·
FDA Recalls
Rohto Cooling Eye Drops Dry Aid Recall Issued
FDA ·
FDA Recalls
Xylocaine Lidocaine HCl Injection Recall Issued
FDA ·
FDA Recalls
Rohto Cooling Eye Drops Digi Eye Recall
FDA ·
FDA Recalls
Levothyroxine Sodium Tablets Recall by Major Pharmaceuticals
FDA ·
FDA Recalls
Levothyroxine Sodium Tablets Recall Issued by Major Pharmaceuticals
FDA ·
FDA Recalls
Levothyroxine Sodium Tablets Recall by Major Pharmaceuticals
FDA ·
FDA Recalls
Naropin Recall Issued for Particulate Matter
FDA ·
FDA Recalls
Levothyroxine Sodium Tablets Recall by Major Pharmaceuticals
FDA ·
FDA Recalls
Levothyroxine Sodium Tablets Recall Due to Subpotency
FDA ·
FDA Recalls
Rohto Cooling Eye Drops Recall
FDA ·
FDA Recalls
Levothyroxine Sodium Tablets Recall for Subpotency
FDA ·
FDA Recalls
Rohto Cooling Eye Drops Max Strength Recall
FDA ·
FDA Recalls high
Abiomed Introducer Kit 23 Fr Recall Due to Leakage Risk
FDA ·
FDA Recalls high
Argon Medical Devices Bone Marrow Tray Recall
FDA ·
FDA Recalls high
Abiomed Impella CP Smart Assist Set Recall
FDA ·
FDA Recalls high
Abiomed Intro Kit Recall Due to Sheath Leakage Risk
FDA ·
FDA Recalls high
Abiomed Impella 5.5 Smart Assist Set Recall
FDA ·
FDA Recalls high
Abiomed Introducer Kit for Impella Recall
FDA ·
FDA Recalls high
Abiomed Impella CP Set Recall Issued
FDA ·
FDA Recalls
3B Medical Recalls Rio II Nasal Pillows Interface
FDA ·
FDA Recalls high
Abiomed Impella RP Flex Recall Due to Sheath Leakage
FDA ·
FDA Recalls
Medtronic DLP One-Piece Pediatric Arterial Cannula Recall
FDA ·
FDA Recalls
da Vinci SP Instrument Arm Drape Recall
FDA ·
FDA Recalls
Medline TOTAL KNEE PACK-LF Kits Recall
FDA ·
FDA Recalls
Olympus Toomey Evacuator 50cc Recall Issued
FDA ·
FDA Recalls
Orthofix MINIRAIL External Fixation Device Recall
FDA ·
FDA Recalls
Optima XR240amx Mobile Digital Radiographic System Recall
FDA ·
FDA Recalls
Vasoview Hemopro 2 Endoscopic Vessel Harvesting System Recall
FDA ·
FDA Recalls high
Abiomed Impella 5.5 SmartAssist S2 Set Recall
FDA ·
FDA Recalls high
Argon Medical Devices Recalls T-Lok Bone Marrow Trays
FDA ·
FDA Recalls
Medtronic Bio-Medicus Adult Cannula Kit Recall
FDA ·
FDA Recalls high
Abiomed Impella CP Introducer Kit Recall
FDA ·
FDA Recalls
Orthofix MINIRAIL Fixator Recall Issued Over Labeling Error
FDA ·
FDA Recalls high
Abiomed Impella CP Set Recall Due to Sheath Leakage
FDA ·
FDA Recalls
Medline TOTAL KNEE PACK Recall
FDA ·
FDA Recalls
Orthofix Articulated Minirail Fixator Recall Due to Labeling Error
FDA ·
FDA Recalls high
Argon Medical Devices Recalls One-Piece Introducer Tray
FDA ·
FDA Recalls
ICU Medical Plum Solo Precision IV Pump Recall
FDA ·
FDA Recalls high
Abiomed Introducer Kit for Impella Recall
FDA ·
FDA Recalls high
Argon Medical Devices Recalls Transvenous Pacing Electrode Trays
FDA ·
FDA Recalls high
Abiomed Insertion Kit Recall Due to Sheath Leakage
FDA ·
FDA Recalls
Daavlin Photera 600 Phototherapy Device Recall
FDA ·
FDA Recalls high
Argon Medical Devices Recalls Arterial Line Kit
FDA ·
FDA Recalls
Olympus Glass Body for 194 Ellik Evacuator Recall
FDA ·
FDA Recalls
Olympus Toomey Evacuator Recalled Over Sterilization Issue
FDA ·
FDA Recalls
Tosoh Bioscience Recalls ST AIA-Pack Testosterone
FDA ·
FDA Recalls high
Argon Medical Devices Recalls General Biospy Tray
FDA ·
FDA Recalls
Optima XR220amx Mobile Radiographic System Recall
FDA ·
FDA Recalls
Photera 400 Phototherapy Device Recall
FDA ·
FDA Recalls high
Abiomed Introducer Kit for Impella Recall
FDA ·
FDA Recalls
Olympus Ellik Evacuator Recall Issued
FDA ·
FDA Recalls high
Abiomed Impella CP Introducer Kit Recall
FDA ·
FDA Recalls
Optima XR200amx Recall Issued by GE Medical Systems
FDA ·
FDA Recalls
Photera 600 3-D Phototherapy Device Recall
FDA ·
FDA Recalls
ICU Medical Plum Duo Infusion Pump Recall
FDA ·
FDA Recalls high
Abiomed Impella CP Introducer Kit Recall
FDA ·
FDA Recalls
Papablic Replacement Brush Heads Recall
FDA ·
FDA Recalls
Papablic Replacement Brush Heads Recall
FDA ·
FDA Recalls high
Abiomed Impella CP Set Recall Due to Leakage Risk
FDA ·
FDA Recalls
Boston Scientific Rapid Refill Continuous Injection System Recall
FDA ·
FDA Recalls
Orthofix MINIRAIL External Fixation Device Recall
FDA ·
FDA Recalls high
D'Dioses Guayaba Ice Pop Recall
FDA ·
FDA Recalls
Pillsbury Kaiser Roll Dough Recall for Potential Glass
FDA ·
FDA Recalls
Pillsbury Bread Rolls Recall Due to Potential Glass
FDA ·
FDA Recalls high
D'Dioses Rompope Ice Pop Recall for Undeclared Allergens
FDA ·
FDA Recalls
Winfield's CWB Chocolate Bars Recalled for Undeclared Milk
FDA ·
FDA Recalls high
D'Dioses Coconut Ice Pop Recall Due to Undeclared Allergens
FDA ·
FDA Recalls
WY Duck Sauce Recall Due to Potential Metal Fragments
FDA ·
FDA Recalls high
D'Dioses Vainilla Ice Pop Recall Issued by FDA
FDA ·
FDA Recalls high
D'Dioses Grocella Ice Pops Recall Issued by FDA
FDA ·
FDA Recalls high
D'Dioses Mamey Ice Pop Recall for Undeclared Allergens
FDA ·
FDA Recalls
Amy's Organic Soups Lentil Light in Sodium Recall
FDA ·
FDA Recalls high
D'Dioses Nanche Ice Pop Recall Due to Undeclared Allergens
FDA ·
FDA Recalls
Functional Formularies Nourish Organic Meal Replacement Recalled
FDA ·
FDA Recalls high
D'Dioses Pina Colada Ice Pops Recall
FDA ·
FDA Recalls high
Organic Whole Blueberries Recall for E. coli Contamination
FDA ·
FDA Recalls high
D'Dioses Pistachio Ice Pop Recall Issued for Undeclared Allergens
FDA ·
FDA Recalls high
D'Dioses Cookies Cream Ice Pop Recall for Undeclared Allergens
FDA ·
FDA Recalls high
D'Dioses Limon Ice Pop Recall Issued for Undeclared Allergens
FDA ·
FDA Recalls high
D'Dioses Mango Ice Pop Recall for Undeclared Allergens
FDA ·
FDA Recalls high
D'Dioses Fresa Leche Ice Pop Recall for Undeclared Allergens
FDA ·
FDA Recalls
Ruby Artichoke Hearts Recall Due to Glass
FDA ·
FDA Recalls
OLA-OLA Pounded Groundnuts Recall for Undeclared Peanuts
FDA ·
FDA Recalls high
D'Dioses Arroz con Leche Ice Pops Recall Issued
FDA ·
FDA Recalls
Nutricia North America Recalls Liquid Hope Organic Meal Replacement
FDA ·
FDA Recalls high
D'Dioses Tamarindo Ice Pop Recall for Undeclared Allergens
FDA ·
FDA Recalls high
D'Dioses Nuez Ice Pop Recall for Undeclared Allergens
FDA ·
FDA Recalls
Foster & Thrive Carbamide Peroxide Recall Issued
FDA ·
FDA Recalls
Good Neighbor Pharmacy Earwax Removal Recall
FDA ·
FDA Recalls
Audiologist's Choice Earwax Removal System Recall
FDA ·
FDA Recalls
TopCare Earwax Removal Kit Recall Issued
FDA ·
FDA Recalls
CVS Health Earwax Removal Drops Recall
FDA ·
FDA Recalls
Meijer Earwax Removal Kit Recall
FDA ·
FDA Recalls
Nystatin Cream Recall Due to Subpotent Drug
FDA ·
FDA Recalls
CAREONE Earwax Removal Drops Recall Announced
FDA ·
FDA Recalls
BD ChloraPrep Clear Recall Due to Sterility Issue
FDA ·
FDA Recalls
Family Wellness Earwax Removal Kit Recall
FDA ·
FDA Recalls
Leader Earwax Removal Kit Recall Due to Subpotent Drug
FDA ·
FDA Recalls
Clinere Ear Wax Remover Recall
FDA ·
FDA Recalls
Quality Choice Earwax Removal Products Recall
FDA ·
FDA Recalls
CLEVIPREX Recall Issued for Sterility Concerns
FDA ·
FDA Recalls
Integra LifeSciences Recalls OmniTract Surgical Retractor System
FDA ·
FDA Recalls
Medline Convenience Kits Recall (Z-2696-2026)
FDA ·
FDA Recalls
EMPOWR 3D KNEE Recall Issued for Packaging Discrepancy
FDA ·
FDA Recalls
EMPOWR 3D KNEE Recall Due to Packaging Discrepancy
FDA ·
FDA Recalls
Medline Open Heart Peds Pack Kits Recall
FDA ·
FDA Recalls
Boston Scientific Intracept Access Instruments Recall
FDA ·
FDA Recalls
VITEK 2 AST-N447 TEST KIT Recall
FDA ·
FDA Recalls
Think Surgical TMINI Tracking Arrays Recall
FDA ·
FDA Recalls
Elekta Geneva Brachytherapy Applicator Recall
FDA ·
FDA Recalls
Elekta Advanced Gynecological Applicator Recall
FDA ·
FDA Recalls
Fresenius 5008X Blood Tubing Sets Recall
FDA ·
FDA Recalls
Elekta Fletcher CT/MR Shielded Applicator Set Recall
FDA ·
FDA Recalls
Siemens Atellica CH Enzymatic Hemoglobin A1c Recall
FDA ·
FDA Recalls
Medline Anesthesia Kit Recall Issued
FDA ·
FDA Recalls
Versius Surgical System Recall Due to Cybersecurity Risk
FDA ·
FDA Recalls
Olympus Single Use Distal Cover Recall
FDA ·
FDA Recalls
Medtronic MiniMed 780G Insulin Pump Recall
FDA ·
FDA Recalls
Klowen Braces Recalls KL Owen Custom Orthodontic Solution
FDA ·
FDA Recalls
GSP Neonatal GALT Kit Recall Issued by Wallac Oy
FDA ·
FDA Recalls
ConvaTec Aquacel Ag Surgical SP Dressing Recall
FDA ·
FDA Recalls
Johnny's Salad and Pasta Elegance Recall for Undeclared Sesame
FDA ·
FDA Recalls high
Fresh & Ready Foods LLC Recalls Fresh to You Burger Chicken Fillet Deluxe with Bacon
FDA ·
FDA Recalls high
High Valley Orchard Chocolate Covered Raisins Recall
FDA ·
FDA Recalls high
Adams Extract & Spice LLC Recalls JB Chicken Sknls for Undeclared Sesame
FDA ·
FDA Recalls
Wondermade Alabama Banana Pudding Marshmallow Recall
FDA ·
FDA Recalls high
Fresh to You Burger Chicken Fillet Recall
FDA ·
FDA Recalls high
Coopers Bbq 60 Gal Bean Mix Box Recall
FDA ·
FDA Recalls
Specialty Bakers Recalls Vanilla Dessert Shells Over Undeclared Soy
FDA ·
FDA Recalls high
Trafa Pharmaceutical Inc. Organic Moringa Leaf Powder Recall
FDA ·
FDA Recalls
Wise Onion Rings Recall for Undeclared Dyes
FDA ·
FDA Recalls high
Adams Extract & Spice LLC Recalls EC Hot Links Seasoning
FDA ·
FDA Recalls
Bakr Brown Butter Chocolate Chunk Cookie Dough Recall
FDA ·
FDA Recalls high
Adams Extract & Spice LLC Recalls Smoked Sausage Spice
FDA ·
FDA Recalls
QuVa Pharma Methohexital Sodium Recall
FDA ·
FDA Recalls
Drogueria San Juan Isopropyl Alcohol Recall
FDA ·
FDA Recalls
Medline Remedy Specialized Silicone Cream Recall
FDA ·
FDA Recalls
Azacitidine for Injection Recall Issued by Reliance Life Sciences
FDA ·
FDA Recalls
Pemetrexed for Injection Recall Due to Sterility Issues
FDA ·
FDA Recalls
Bortezomib for Injection Recall Issued by Reliance Life Sciences
FDA ·
FDA Recalls
Drogueria San Juan Isopropyl Alcohol 70% Recall
FDA ·
FDA Recalls
Gasco Isopropyl Alcohol 70% Recall Issued
FDA ·
FDA Recalls
Pemetrexed for Injection Recall Issued by Reliance Life Sciences
FDA ·
FDA Recalls
Shimoga Chemicals Recalls Clomiphene Citrate API
FDA ·
FDA Recalls
Drogueria San Juan Isopropyl Alcohol Recall Issued
FDA ·
FDA Recalls
Gasco Isopropyl Alcohol 70% Recall for Subpotency
FDA ·
FDA Recalls
Gasco Isopropyl Alcohol 70% Recall Issued
FDA ·
FDA Recalls
Methohexital Sodium for Injection Recall Issued
FDA ·
FDA Recalls high
Hillrom VOLARA P.CIRCUIT 5KIT Recall Issued by Baxter
FDA ·
FDA Recalls
Medline L&D Continuous Epidural Tray Recall
FDA ·
FDA Recalls
Medline Convenience Kits Recall Due to Lidocaine Quality Issues
FDA ·
FDA Recalls high
Hillrom VOLARA System P.CIRCUIT KIT Recall Issued
FDA ·
FDA Recalls
Siemens ARTIS icono ceiling Recall
FDA ·
FDA Recalls
Power-Trialysis Dialysis Catheters Recall Issued by Bard Access Systems
FDA ·
FDA Recalls high
Omnipod (Eros) Pod Recall Issued by Insulet Corporation
FDA ·
FDA Recalls
Hamilton Medical IntelliCuff Device Recall
FDA ·
FDA Recalls
MEDLINE 111 Gravity Set Recall Issued
FDA ·
FDA Recalls
Medacta Short Monobloc Stem Broaches Recall
FDA ·
FDA Recalls
Boston Scientific Recalls CRE Pro Wireguided Devices
FDA ·
FDA Recalls
Zimmer Surgical Recalls Sterile Tourniquet Hoses
FDA ·
FDA Recalls high
Aligned Medical Solutions Preop Kit-NS Recall
FDA ·
FDA Recalls high
Aligned Medical Solutions DSAEK Pack-RX Recall
FDA ·
FDA Recalls
Bard Access Systems PowerPICC Catheters Recall
FDA ·
FDA Recalls
Boston Scientific CRE Wireguided Recall Issued
FDA ·
FDA Recalls
Solar GI System Recall Issued by Laborie Medical Technologies
FDA ·
FDA Recalls high
Medline Industries Recalls Reprocessed Electrophysiology Catheters
FDA ·
FDA Recalls
Medline Circumcision Trays Recall Due to Lidocaine Quality Issues
FDA ·
FDA Recalls
Medline Arterial Line Kit and IV Securement Set Recall
FDA ·
FDA Recalls
Siemens ARTIS icono biplane Recall Issued
FDA ·
FDA Recalls high
Medtronic Harmony Delivery Catheter System Recall
FDA ·
FDA Recalls
Bard Access Systems Soft Tissue Biopsy Trays Recall
FDA ·
FDA Recalls
Boston Scientific Recalls CRE Pro Wireguided Devices
FDA ·
FDA Recalls
Masimo Radius VSM Disposable NIBP Cuff Recall
FDA ·
FDA Recalls
Medline Ophthalmic Pack W/Lido Recall Issued
FDA ·
FDA Recalls
Accuray Cyberknife Treatment Deliver System Recall
FDA ·
FDA Recalls
Medline Convenience Kits Recall Involving Swan-Ganz Catheters
FDA ·
FDA Recalls
Medline Right Heart Cath Pack CTX Recall
FDA ·
FDA Recalls
Depuy Synthes ATTUNE Revision Hinge Knee Recall
FDA ·
FDA Recalls
Boston Scientific CRE Wireguided Recall
FDA ·
FDA Recalls
Bard Access Systems PowerMidline Catheter Recall
FDA ·
FDA Recalls
Boston Scientific Recalls CRE Wireguided Devices
FDA ·
FDA Recalls
Bard Access Systems Groshong NXT ClearVue Catheter Recall
FDA ·
FDA Recalls high
Hillrom VOLARA System Circuit Recall Issued
FDA ·
FDA Recalls high
Aligned Medical Solutions Thyroid FNA Pack-RX Recall
FDA ·
FDA Recalls
Bard Access Systems Recalls Acute Drainage Trays
FDA ·
FDA Recalls
Depuy Synthes ATTUNE Revision Hinge Knee Inserts Recall
FDA ·
FDA Recalls
Siemens ARTIS icono floor Recall Issued
FDA ·
FDA Recalls
Zimmer Surgical Recalls Sterile Tourniquet Hoses
FDA ·
FDA Recalls high
Dr. Lewin Pack Surgical Kit Recall
FDA ·
FDA Recalls
Medline BLOCK TRAY Kits Recall
FDA ·
FDA Recalls
Boston Scientific CRE Wireguided Recall
FDA ·
FDA Recalls
Boston Scientific CRE Wireguided Recall
FDA ·
FDA Recalls
Medline Lumbar Puncture Choice Kits Recall
FDA ·
FDA Recalls high
Omnipod DASH Pod Recall Issued by Insulet Corporation
FDA ·
FDA Recalls
Baxter Adapter for Head Positioning Recall
FDA ·
FDA Recalls
Medline Convenience Kits Recall Due to Swan-Ganz Catheter Issues
FDA ·
FDA Recalls
Accuray Cyberknife Treatment Delivery System Recall
FDA ·
FDA Recalls
PowerPICC SOLO HF Catheter Recall by Bard Access Systems
FDA ·
FDA Recalls
Boston Scientific CRE Wireguided Recall
FDA ·
FDA Recalls high
Hamilton Medical Coaxial Breathing Circuit Sets Recall
FDA ·
FDA Recalls
Medline Convenience Kits Recall Issued by FDA
FDA ·
FDA Recalls
Boston Scientific Recalls CRE Pro Wireguided Devices
FDA ·
FDA Recalls
GORE TAG Thoracic Branch Endoprosthesis Side Branch Component Recall
FDA ·
FDA Recalls
Mentor B9604 Syringe Recall (Z-2614-2026)
FDA ·
FDA Recalls
Covidien Shiley Disposable Decannulation Plug Recall
FDA ·
FDA Recalls
Boston Scientific CRE Pro Wireguided Recall
FDA ·
FDA Recalls
Bard Access Systems Recalls PowerPICC SV Catheters
FDA ·
FDA Recalls
Medela ENFit ExSet Strl 60 2.0ml PV Recall
FDA ·
FDA Recalls
Siemens ARTIS icono ceiling Recall
FDA ·
FDA Recalls
Boston Scientific CRE Pro Wireguided Recall Due to Sterile Breach
FDA ·
FDA Recalls
RayCare 2024A SP4 Oncology Information Systems Recall
FDA ·
FDA Recalls
Medline Convenience Kits Recall
FDA ·
FDA Recalls
Medline Convenience Kits Recall Involving Swan-Ganz Catheters
FDA ·
FDA Recalls
Medline Convenience Kits Recall Due to Lidocaine Quality Issues
FDA ·
FDA Recalls high
Baxter Recalls Hillrom VOLARA System Circuit Kits
FDA ·
FDA Recalls
Bard Access Systems Recalls PowerPICC Provena Catheters
FDA ·
FDA Recalls
Bard Access Systems Recalls DuoGlide Dialysis Catheter
FDA ·
FDA Recalls
Bard Access Systems Recalls Provena Midline Catheters
FDA ·
FDA Recalls
Medline Suturing Set Recall Due to Lidocaine Quality Issues
FDA ·
FDA Recalls
Medline Convenience Kits Recall Due to Lidocaine Quality Issues
FDA ·
FDA Recalls
Bard Access Systems PowerMidline Catheter Recall
FDA ·
FDA Recalls
Medline Convenience Kits Recall Involves Swan-Ganz Catheters
FDA ·
FDA Recalls high
Omnipod 5 Pods Recall Due to Insulin Leak Risk
FDA ·
FDA Recalls
Zeiss Intrabeam Spherical Applicator Recall
FDA ·
FDA Recalls
Medline Convenience Kits Recall Due to Swan-Ganz Catheters
FDA ·
FDA Recalls
Medline Convenience Kits Recall
FDA ·
FDA Recalls
Medline Convenience Kits Recall Due to Lidocaine Quality Issues
FDA ·
FDA Recalls
Bard Access Systems Recalls Power-Trialysis Slim-Cath Dialysis Catheters
FDA ·
FDA Recalls
Masimo Radius VSM ECG Pre-Connected Set Recall
FDA ·
FDA Recalls
Medline Convenience Kits Recall Due to Lidocaine Quality Issues
FDA ·
FDA Recalls
Pilling Wecksorb Neurosponges Recall Due to Endotoxin Levels
FDA ·
FDA Recalls
Boston Scientific Recalls CRE Pro Wireguided Devices
FDA ·
FDA Recalls
Medline Convenience Kits Recall Involving Swan-Ganz Catheters
FDA ·
FDA Recalls
Bard Access Systems Poly Midline Catheter Recall
FDA ·
FDA Recalls
RayCare 2024A SP1 Oncology Information Systems Recall
FDA ·
FDA Recalls
Medline Convenience Kits Recall Involving Swan-Ganz Catheters
FDA ·
FDA Recalls
Remel GC Agar Base Recall Issued for Reduced Bacterial Recovery
FDA ·
FDA Recalls
MorningStar Farms Sausage Patties Recall
FDA ·
FDA Recalls high
Nara Organics Infant Formula Recall
FDA ·
FDA Recalls
Ocular Plus Dietary Supplement Recall for Undeclared Yellow#5
FDA ·
FDA Recalls
Vista MAX Dietary Supplement Recall for Undeclared Yellow #5
FDA ·
FDA Recalls high
FIRST STREET Dark Chocolate Raisins Recall for Undeclared Peanuts
FDA ·
FDA Recalls high
MOGO Pure Moringa Oleifera Capsules Recall
FDA ·
FDA Recalls
Fry Pie Factory LLC Pepperoni Rolls Recall
FDA ·
FDA Recalls
MorningStar Farms Buffalo Chik'n Nuggets Recall
FDA ·
FDA Recalls
Synjardy XR Tablets Recall Issued
FDA ·
FDA Recalls
Lannett Recalls Dextroamphetamine Extended-Release Capsules
FDA ·
FDA Recalls
BD ChloraPrep Clear Recall Due to Sterility Concerns
FDA ·
FDA Recalls
BD ChloraPrep Hi-Lite Orange Recall for Sterility Assurance
FDA ·
FDA Recalls
BD ChloraPrep Scrub Teal Recall for Sterility Assurance Issue
FDA ·
FDA Recalls
BD ChloraPrep Hi-Lite Orange Recall Due to Sterility Concerns
FDA ·
FDA Recalls
IMULDOSA Injection Recall Due to Sterility Concerns
FDA ·
FDA Recalls
Lidocaine HCl Injection USP Recall Issued
FDA ·
FDA Recalls
Cinacalcet Hydrochloride Tablets Recall Due to Impurity
FDA ·
FDA Recalls
Cinacalcet Hydrochloride Tablets Recall Due to Impurity
FDA ·
FDA Recalls
BD PurPrep Applicators Recalled for Sterility Issues
FDA ·
FDA Recalls
Accord Healthcare Levothyroxine Sodium Tablets Recall
FDA ·
FDA Recalls
BD ChloraPrep Scrub Teal Recall Issued for Sterility Concerns
FDA ·
FDA Recalls
Lupin Prednisolone Acetate Ophthalmic Suspension Recall
FDA ·
FDA Recalls
BD ChloraPrep Clear Recall Due to Sterility Issue
FDA ·
FDA Recalls
BD ChloraPrep Clear Recall Due to Sterility Issues
FDA ·
FDA Recalls
Accucaine Lidocaine Kit Recall Due to Sterility Concerns
FDA ·
FDA Recalls
Cinacalcet Hydrochloride Tablets Recall Issued by Cipla USA
FDA ·
FDA Recalls
ChloraPrep FREPP Recall Due to Sterility Issue
FDA ·
FDA Recalls
BD ChloraPrep Hi-Lite Orange Recall Due to Sterility Issues
FDA ·
FDA Recalls
Philips Telemetry Monitor 5500 Recall
FDA ·
FDA Recalls
Zimmer Off-Axis Reamer Guide Recall
FDA ·
FDA Recalls
Surgify Halo Drill Recall Issued for Burr Breakage Risk
FDA ·
FDA Recalls
Surgify Halo Drill Recall Issued by FDA
FDA ·
FDA Recalls
Zimmer Off-Axis Shoulder System Reamer Guide Recall
FDA ·
FDA Recalls
Acumed Hexalob Screws Recall Due to Breakage Risk
FDA ·
FDA Recalls
Zimmer Off-Axis Alliance Glenoid Recall
FDA ·
FDA Recalls
Medline Convenience Kits Recall for Unapproved Design Changes
FDA ·
FDA Recalls
Medline Convenience Kits Recall for Unapproved Design Changes
FDA ·
FDA Recalls
Medline Convenience Kits Recall Issued for Unapproved Design Changes
FDA ·
FDA Recalls high
Abiomed Impella CP Set with SmartAssist Recall
FDA ·
FDA Recalls
Medline Convenience Kits Recall for Unapproved Design Changes
FDA ·
FDA Recalls
Surgify Halo Drill Recall Issued by FDA
FDA ·
FDA Recalls
Surgify Halo Drill Recall Issued for Burr Breakage Risk
FDA ·
FDA Recalls
Surgify Halo 3.0 mm Drill Recall Issued for Breakage Risk
FDA ·
FDA Recalls
Surgify Halo Drill Recall Issued by FDA
FDA ·
FDA Recalls
Medline Convenience Kits Recall for Unapproved Design Changes
FDA ·
FDA Recalls
Medline Convenience Kits Recall for Unapproved Design Changes
FDA ·
FDA Recalls
Surgify Halo Drill Recall Issued for Burr Breakage Risk
FDA ·
FDA Recalls high
Medline Convenience Kits Recall
FDA ·
FDA Recalls
TMJ Bilateral Implants Recall Issued by TMJ Solutions Inc
FDA ·
FDA Recalls high
Medline Convenience Kits Recall
FDA ·
FDA Recalls
Surgify Halo Drill Recall Issued Over Burr Breakage Risk
FDA ·
FDA Recalls
Surgify Halo Drill Recall Issued for Burr Breakage Risk
FDA ·
FDA Recalls
Philips Avalon Fetal Monitor Recall Issued
FDA ·
FDA Recalls
Medtronic Octopus Evolution Tissue Stabilizer Recall
FDA ·
FDA Recalls
GE Healthcare AW Server 3.2 Recall for Synchronization Issue
FDA ·
FDA Recalls
Medline Convenience Kits Recall for Unapproved Design Changes
FDA ·
FDA Recalls
Surgify Halo Drill Recall Due to Burr Breakage Risk
FDA ·
FDA Recalls
Medline Major Basin Set Kits Recall
FDA ·
FDA Recalls high
Medline Convenience Kits Recall Issued
FDA ·
FDA Recalls
Medline Convenience Kits Recall for Unapproved Design Changes
FDA ·
FDA Recalls
Medline Convenience Kits Recall Due to Design Changes
FDA ·
FDA Recalls
Medline Convenience Kits Recall for Unapproved Syringe Design
FDA ·
FDA Recalls
Surgify Halo Drill Recall Issued for Burr Breakage Risk
FDA ·
FDA Recalls
PFM Medical Multi-Snare Set Recall Issued
FDA ·
FDA Recalls high
Medline Convenience Kits Recall
FDA ·
FDA Recalls
Medline Convenience Kits Recall
FDA ·
FDA Recalls
Surgify Halo Drill Recall for Potential Burr Breakage
FDA ·
FDA Recalls high
Abiomed Impella Introducer Kit Recall
FDA ·
FDA Recalls
Zimmer Persona Revision Femoral Distal Augment Recall
FDA ·
FDA Recalls
Thuvera Laser Console Recall Issued by IPG Medical
FDA ·
FDA Recalls
Boston Scientific Recalls INTERA 3000 Hepatic Artery Infusion Pump
FDA ·
FDA Recalls
Medline Convenience Kits Recall Issued
FDA ·
FDA Recalls
Surgify Halo Recall Issued for Potential Burr Breakage
FDA ·
FDA Recalls
Octopus 4 Tissue Stabilizer Recall
FDA ·
FDA Recalls
Da Vinci ASSY PSS SP1098 Recall
FDA ·
FDA Recalls
Stryker Neurovascular Recalls INZONE DETACHMENT SYSTEM
FDA ·
FDA Recalls
Surgify Halo Drill Recall Issued for Burr Breakage Risk
FDA ·
FDA Recalls high
Abiomed Impella Introducer Kit Recall
FDA ·
FDA Recalls
Zimmer Off-Axis Alliance Glenoid Reamer Guide Recall
FDA ·
FDA Recalls
Octopus Evolution AS Tissue Stabilizer Recall
FDA ·
FDA Recalls
Surgify Halo Drill Recall Due to Potential Burr Breakage
FDA ·
FDA Recalls
Surgify Halo Drill Recall Issued by FDA
FDA ·
FDA Recalls
Philips Avalon Fetal Monitor Recall Due to Speaker Issue
FDA ·
FDA Recalls
Medline Convenience Kits Recall for Unapproved Design Changes
FDA ·
FDA Recalls
Surgify Halo Drill Recall Issued for Burr Breakage Risk
FDA ·
FDA Recalls high
Abiomed Impella CP Set with SmartAssist Recall
FDA ·
FDA Recalls
Medline Convenience Kits Recall Over Unapproved Design Changes
FDA ·
FDA Recalls
Medline Convenience Kits Recall for Unapproved Design Changes
FDA ·
FDA Recalls
Ventec Life Systems VOCSN+Pro Recall
FDA ·
FDA Recalls
Zimmer Off-Axis Reamer Guide Recall
FDA ·
FDA Recalls
Surgify Halo Drill Recall Issued for Burr Breakage Risk
FDA ·
FDA Recalls
Dexcom G7 Continuous Glucose Monitoring System Recall
FDA ·
FDA Recalls
Surgify Halo Burrs Recall for Breakage Risk
FDA ·
FDA Recalls high
George J Howe Recalls Sunflower Seeds for Undeclared Cashew
FDA ·
FDA Recalls
Boichik Bagels Tuna Salad Recall for Allergen Labeling Error
FDA ·
FDA Recalls
Joy Peach Lassi Recall Issued for Inadequate Pasteurization
FDA ·
FDA Recalls
Joy Salty Lassi Recall Issued for Pasteurization Issue
FDA ·
FDA Recalls high
George J Howe Company Recalls Sunflower Seeds
FDA ·
FDA Recalls high
Zapp's Bayou Blackened Ranch Potato Chips Recall
FDA ·
FDA Recalls
Joy Mint Lassi Recall Issued for Inadequate Pasteurization
FDA ·
FDA Recalls high
Spring & Mulberry Pecan Date Chocolate Recall
FDA ·
FDA Recalls
Boichik Bagels Whitefish Salad Recall Due to Allergen Labeling
FDA ·
FDA Recalls high
Spring & Mulberry Chocolate Recall for Potential Salmonella
FDA ·
FDA Recalls high
George J Howe Company Recalls Sunflower Seed Tub for Undeclared Cashew
FDA ·
FDA Recalls high
George J Howe Company Recalls 5# Sunflower Seeds C/S
FDA ·
FDA Recalls
Joy Orange Lassi Recall Due to Inadequate Pasteurization
FDA ·
FDA Recalls high
Spring & Mulberry Chocolate Recall Over Salmonella Risk
FDA ·
FDA Recalls high
Pearl Milling Company Pancake Mix Recall for Undeclared Allergens
FDA ·
FDA Recalls high
Spring & Mulberry Mint Leaf Date-Sweetened Chocolate Recall
FDA ·
FDA Recalls high
Zapp's Big Cheezy Potato Chips Recall
FDA ·
FDA Recalls high
Spring & Mulberry Coffee Date-Sweetened Chocolate Recall
FDA ·
FDA Recalls high
Spring & Mulberry Earl Grey Chocolate Recall
FDA ·
FDA Recalls
El David Gelee Bonbons Recall for Undeclared Colors
FDA ·
FDA Recalls
Joy Strawberry Lassi Recall Due to Pasteurization Issue
FDA ·
FDA Recalls high
Spring & Mulberry Mixed Berry Date-Sweetened Chocolate Recall
FDA ·
FDA Recalls
Joy Mango Lassi Recall Issued for Inadequate Pasteurization
FDA ·
FDA Recalls high
Spring & Mulberry Chocolate Recall Over Salmonella Risk
FDA ·
FDA Recalls high
Spring & Mulberry Sea Salt Date-Sweetened Chocolate Recall
FDA ·
FDA Recalls
Joy Masala Chaash Lassi Recall Issued for Pasteurization Issue
FDA ·
FDA Recalls
Joy Mango-Pina-Strawberry Lassi Recall Issued
FDA ·
FDA Recalls high
Utz Quality Foods Recalls Dirty Maui Onion Chips
FDA ·
FDA Recalls
Joy Sweet Lassi Recall Issued for Inadequate Pasteurization
FDA ·
FDA Recalls
Produce Innovations Sandwich Recall for Incorrect Labeling
FDA ·
FDA Recalls high
25# Sunflower Seeds C/S Recalled for Undeclared Cashew Allergen
FDA ·
FDA Recalls
Joy Rose Lassi Recall Issued for Inadequate Pasteurization
FDA ·
FDA Recalls high
Spring & Mulberry Chocolate Recall Over Salmonella Risk
FDA ·
FDA Recalls high
George J Howe Company Recalls Sunflower Seeds
FDA ·
FDA Recalls high
Spring & Mulberry Mango Chili Chocolate Recall
FDA ·
FDA Recalls
Joy Saffron Cardamon Lassi Recall Issued by Joy Gourmet Foods LLC
FDA ·
FDA Recalls
Motor City Pizza Co. 5 Cheese Bread Recall
FDA ·
FDA Recalls high
Zapp's Bayou Blackened Ranch Kettle Chips Recall
FDA ·
FDA Recalls high
Utz Dirty Sour Cream and Onion Potato Chips Recall
FDA ·
FDA Recalls
Boichik Bagels Pumpernickel Mix Bagels Recall for Undeclared Sesame
FDA ·
FDA Recalls high
Dirty Brand Salt and Vinegar Potato Chips Recall
FDA ·
FDA Recalls high
Prime Food Processing LLC Recalls Dried Herring Fish
FDA ·
FDA Recalls
Joy Pineapple Lassi Recall Issued for Inadequate Pasteurization
FDA ·
FDA Recalls high
BD ChloraPrep FREPP Clear Recall Issued by FDA
FDA ·
FDA Recalls
Sensipar Tablets Recall Due to CGMP Deviations
FDA ·
FDA Recalls
Sensipar Tablets Recall Due to CGMP Deviations
FDA ·
FDA Recalls
Sun Pharmaceutical Recalls Perampanel 6mg Tablets
FDA ·
FDA Recalls
Hydroxyzine Hydrochloride Oral Solution Recall by ANI Pharmaceuticals
FDA ·
FDA Recalls high
BD ChloraPrep Clear Applicators Recall Issued for Non-Sterility
FDA ·
FDA Recalls
PReye Vitamin See Eye Drops Recall Issued
FDA ·
FDA Recalls
Major Methylergonovine Maleate Tablets Recall
FDA ·
FDA Recalls
Central Admixture Pharmacy Services Recalls Pediatric TPN Bag
FDA ·
FDA Recalls
BD ChloraPrep FREPP Clear Recall Due to Sterility Issue
FDA ·
FDA Recalls
Direct Rx Duloxetine Recall for N-Nitroso Impurity
FDA ·
FDA Recalls
Povi-One Oral Antiseptic Recall Due to Sub Potency
FDA ·
FDA Recalls
Sensipar Tablets Recall Issued for CGMP Deviations
FDA ·
FDA Recalls
Fenofibrate Capsules Recall Due to CGMP Deviations
FDA ·
FDA Recalls
BD ChloraPrep Clear Recall Due to Sterility Concerns
FDA ·
FDA Recalls
Amgen Recalls Corlanor Tablets Over Foreign Substance
FDA ·
FDA Recalls
Corlanor Tablets Recalled for Foreign Substance
FDA ·
FDA Recalls
Lacosamide Tablets Recall Due to Foreign Tablet Mix-Up
FDA ·
FDA Recalls
Steris HarmonyAIR A-Series Surgical Lighting System Recall
FDA ·
FDA Recalls high
Arrow International Recalls Drainage and Thoracentesis Kits
FDA ·
FDA Recalls high
Abiomed Automated Impella Controller Recall
FDA ·
FDA Recalls high
Arrow International Recalls PSI and MAC Kits
FDA ·
FDA Recalls
Medline Medical Procedure Kits Recall
FDA ·
FDA Recalls
Medline Medical Procedure Kits Recall
FDA ·
FDA Recalls
Medline Industries Recalls Medical Procedure Kits Due to Catheter Issues
FDA ·
FDA Recalls
ConMed AirSeal Access Port Recall Issued for Overpressure Alerts
FDA ·
FDA Recalls
Medline Pre-connected Urethral Catheterization Tray Recall
FDA ·
FDA Recalls
BD Connecta BD Luer-Lok 360 Stopcock Recall
FDA ·
FDA Recalls
Medline Convenience Kits Recall Due to Adhesive Tubing Issue
FDA ·
FDA Recalls
Medline Urethral Catheterization Tray Recall Issued
FDA ·
FDA Recalls high
Arrow International Recalls Arterial Line Kits and RA Cath Kits
FDA ·
FDA Recalls
Medline Convenience Kits Recall
FDA ·
FDA Recalls
Medline Urethral Catheterization Tray Recall
FDA ·
FDA Recalls
STAAR ICL Calculation Software Recall
FDA ·
FDA Recalls high
Arrow International Recalls CVC Kits
FDA ·
FDA Recalls
Triathlon Universal Baseplate Size 4 Recall Issued
FDA ·
FDA Recalls
Medline Convenience Kits Recall
FDA ·
FDA Recalls
Medline Urethral Catheters Recall Issued
FDA ·
FDA Recalls high
Datex-Ohmeda Panda Freestanding Warmer Recall
FDA ·
FDA Recalls
Medline Convenience Kits Recall Due to Adhesive Tubing Issue
FDA ·
FDA Recalls
Medline HYSTERECTOMY PACK-LF Kits Recall
FDA ·
FDA Recalls high
Arrow International Kits Recall
FDA ·
FDA Recalls
Medline Convenience Kits Recall Issued
FDA ·
FDA Recalls
HeartMate HM 11V Li-ion Backup Battery Recall
FDA ·
FDA Recalls high
Arrow International Recalls Biopsy System Comprehensive Kits
FDA ·
FDA Recalls
Medline Convenience Kits Recall
FDA ·
FDA Recalls
Medline Medical Procedure Kits Recall
FDA ·
FDA Recalls high
Mito Red Light Super Mobile Recall Issued for Battery Fire Risk
FDA ·
FDA Recalls
Medline Medical Procedure Kits Recall
FDA ·
FDA Recalls high
Arrow International Recalls Arterial Catheter Kits
FDA ·
FDA Recalls
Medline Medical Procedure Kits Recall
FDA ·
FDA Recalls high
ARROW INTERNATIONAL Recalls Pacing/PSI Kit
FDA ·
FDA Recalls
Steris HarmonyAIR A-Series Surgical Lighting System Recall
FDA ·
FDA Recalls
ConMed AirSeal Access Port Recall Issued
FDA ·
FDA Recalls high
Arrow International Recalls CVC Kits Due to Potential Sterility Issues
FDA ·
FDA Recalls
Medline Nerve Block Trays Recall Due to Adhesive Tubing Issue
FDA ·
FDA Recalls high
Arrow International Recalls Peritoneal Lavage Cath Kit
FDA ·
FDA Recalls
Medline Urology Procedure Kits Recall
FDA ·
FDA Recalls high
Giraffe Warmer and Panda Warmer Recall
FDA ·
FDA Recalls
Medline Nursing Kit Recall Due to Catheter Issues
FDA ·
FDA Recalls
Medline BREAST-HERNIA-PORT CDS-LF Kits Recall
FDA ·
FDA Recalls high
Giraffe Stand-alone Infant Resuscitation System Recall
FDA ·
FDA Recalls high
Arrow International Hemodialysis Kit Recall
FDA ·
FDA Recalls high
Arrow International Catheter Kits Recall
FDA ·
FDA Recalls
ConMed AirSeal Access Port Recall Due to Overpressure Alerts
FDA ·
FDA Recalls high
Arrow International Hemodialysis Kit Recall
FDA ·
FDA Recalls
Medline Medical Procedure Kits Recall
FDA ·
FDA Recalls
Medline Convenience Kits Recall Due to Adhesive Issue
FDA ·
FDA Recalls
Medline Medical Procedure Kits Recall (Z-2492-2026)
FDA ·
FDA Recalls
Inspire Respiratory Sensing Lead Recall
FDA ·
FDA Recalls
Medline Oral Restoration Kits Recall
FDA ·
FDA Recalls
Medline C-SECTION KIT Recall Issued by FDA
FDA ·
FDA Recalls
Medline Intermittent Latex Catheter Recall Issued
FDA ·
FDA Recalls
Medline EBSI Kit Recall Due to Adhesive Tubing Issue
FDA ·
FDA Recalls
Merit Medical Splashwire Hydrophilic Guide Wire Recall
FDA ·
FDA Recalls high
Arrow International SAC Kits Recall
FDA ·
FDA Recalls high
Arrow International Recalls PICC Access Tray (Z-2395-2026)
FDA ·
FDA Recalls high
Arrow International Spinal Anesthesia Kits Recall
FDA ·
FDA Recalls high
Arrow International Recalls AHDC Kits (Z-2374-2026)
FDA ·
FDA Recalls high
Arrow International Recalls Arterial Catheterization Kits
FDA ·
FDA Recalls high
ARROW INTERNATIONAL Recalls Access Tray ASK-04001-MC3
FDA ·
FDA Recalls
Medline Medical Procedure Kits Recall
FDA ·
FDA Recalls
Medline Labor & Delivery C-Section Kits Recall
FDA ·
FDA Recalls
Medline Industries Recalls Cath Lab Packs Over Adhesive Issue
FDA ·
FDA Recalls high
Arrow International Recalls CVC Kits and Access Trays
FDA ·
FDA Recalls
Medline BILAT MICRO VASECTOMY REVERSAL Kits Recall
FDA ·
FDA Recalls
Medline Hernia Repair Tote Kits Recall
FDA ·
FDA Recalls
Medline SMSC-PELVISCOPY PACK-LF Recall Issued
FDA ·
FDA Recalls
Medline WT LAVH PACK Recall Issued by FDA
FDA ·
FDA Recalls
Medline Nerve Block Trays Recall (Z-2416-2026)
FDA ·
FDA Recalls high
Arrow International Recalls PI MIDLINE 2L Kits
FDA ·
FDA Recalls
Medline PELVIC LAP PACK Recall
FDA ·
FDA Recalls
Medline Convenience Kits Recall Due to Adhesive Tubing Issue
FDA ·
FDA Recalls
ConMed AirSeal Access Port Recall Due to Overpressure Alerts
FDA ·
FDA Recalls high
Arrow International Recalls PICC Kits Over Supplier Drug Quality Issues
FDA ·
FDA Recalls high
Arrow International Catheter Kits Recall
FDA ·
FDA Recalls
ConMed AirSeal 5mm Access Port Recall
FDA ·
FDA Recalls
HeartMate 3 LVAS Kits Recall Issued by Thoratec
FDA ·
FDA Recalls
ConMed AirSeal 12mm Access Port Recall
FDA ·
FDA Recalls high
Arrow International Paracentesis Kit Recall
FDA ·
FDA Recalls
Medline Convenience Kits Recall
FDA ·
FDA Recalls
HeartMate 3 System Controller Recall Issued
FDA ·
FDA Recalls
Medline DAVINCI MAIN Kits Recall Issued
FDA ·
FDA Recalls high
Arrow International Recalls PSI Kits and MAC Kits
FDA ·
FDA Recalls
Medline LAPAROSCOPY COMBINED - NO NDL Kits Recall
FDA ·
FDA Recalls high
Arrow International Hemodialysis Kits Recall
FDA ·
FDA Recalls
Triathlon Universal Baseplate Recall Issued by Howmedica Osteonics
FDA ·
FDA Recalls high
Abiomed Impella CP Set with SmartAssist Recall
FDA ·
FDA Recalls high
Arrow International Epidural Catheterization Kits Recall
FDA ·
FDA Recalls high
Arrow International Recalls PI JACC Kits
FDA ·
FDA Recalls
Inspire Stimulation Lead Recall Issued
FDA ·
FDA Recalls
Medtronic O-arm O2 Imaging System Recall
FDA ·
FDA Recalls
Nutrisystem Chocolate Cheesecake Recall for Undeclared Soy
FDA ·
FDA Recalls
Dairy House Ingredient Systems Strawberry Dairy Powder Recall
FDA ·
FDA Recalls high
White Cheddar Seasoning Recall Issued by Jonco Industries
FDA ·
FDA Recalls
Fairhope Roasting Company Cold Brew Coffee Concentrate Recall
FDA ·
FDA Recalls
United Salt Corp Salt Recall
FDA ·
FDA Recalls
MID DOLCIARIA SRL Recalls Cannoli Siciliani Over Unapproved Colors
FDA ·
FDA Recalls high
Azuma Foods Recalls Tako Wasabi for Undeclared Fish
FDA ·
FDA Recalls
Great Value Hawaiian Roll Recall Issued by United States Bakery
FDA ·
FDA Recalls
Legacy Tex Dressing Stabilizer Blend Recalled for Salmonella
FDA ·
FDA Recalls high
Al Yaman Halawa Extra Pistachio Recall
FDA ·
FDA Recalls
Adndale Magnesium Glycinate Gummies Recall for Undeclared Melatonin
FDA ·
FDA Recalls
Dairy House Vanilla Dairy Powder Recall
FDA ·
FDA Recalls
.155 CRUNCHY CANNOLI GLUTEN FREE Recall Issued
FDA ·
FDA Recalls
Med Pride Bacitracin Zinc Ointment Recall
FDA ·
FDA Recalls
Cura Hongos Antifungal Cream Recall
FDA ·
FDA Recalls
VistaPharm KERR INSTA-CHAR Recall Issued
FDA ·
FDA Recalls
Pearson Topical Anesthetic Gel Recall Due to Defective Containers
FDA ·
FDA Recalls
Buprenorphine HCl Injection Recall
FDA ·
FDA Recalls
Circle K Triple Antibiotic Ointment Recall
FDA ·
FDA Recalls
Alyacen 7/7/7 Recall Issued for Impurity Issues
FDA ·
FDA Recalls
Med Pride Triple Antibiotic Ointment Recall
FDA ·
FDA Recalls
Focalin XR Recall Due to Labeling Issue
FDA ·
FDA Recalls
Med Pride Antifungal Cream Recall Issued
FDA ·
FDA Recalls
safco SensiCaine-Ultra Topical Anesthetic Gel Recall
FDA ·
FDA Recalls
Lil Drug Store Triple Antibiotic Ointment Recall
FDA ·
FDA Recalls
Dental City Topical Anesthetic Gel Recall Issued
FDA ·
FDA Recalls
Burkhart Topical Anesthetic Gel Recall Due to Defective Containers
FDA ·
FDA Recalls
Aripiprazole Tablets USP Recall Due to Product Mix-Up
FDA ·
FDA Recalls
KERR INSTA-CHAR Recall Issued for Monograph Non-Compliance
FDA ·
FDA Recalls
KERR INSTA-CHAR Activated Charcoal Recall
FDA ·
FDA Recalls
Med Pride Bacitracin Zinc Ointment Recall Issued
FDA ·
FDA Recalls
Med Pride Hydrocortisone Cream 1% Recall Issued
FDA ·
FDA Recalls
Lucky Super Soft Antifungal Cream Recall
FDA ·
FDA Recalls
Quala Topical Anesthetic Gel Recall Due to Defective Containers
FDA ·
FDA Recalls
Chlorthalidone Tablets Recall Issued for Failed Dissolution
FDA ·
FDA Recalls
IntegraDose Vasopressin Syringes Recalled for Subpotency
FDA ·
FDA Recalls
Lucky Super Soft Antibiotic Ointment Recall
FDA ·
FDA Recalls
Rapidol Triple Antibiotic Ointment Recall
FDA ·
FDA Recalls
PureLife Topical Anesthetic Gel Recall
FDA ·
FDA Recalls
Med Pride Hydrocortisone Cream Recall Issued
FDA ·
FDA Recalls
DHP Topical Anesthetic Gel Recall Issued
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