FDA Recalls, Food, Drug & Medical Device Alerts - Page 9 of 27
Latest food, drug, and medical device recalls issued by the U.S. Food and Drug Administration. Class I, II, and III recall classifications, affected products, and consumer guidance.
Showing 401–450 of 1,348 FDA recalls. Browse by month →
FDA Recalls
Acella Naproxen Oral Suspension Recall
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FDA Recalls
BD PurPrep Recall Due to Potential Sterility Issues
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FDA Recalls
BD PurPrep Recall Issued by FDA
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FDA Recalls
TPN Bag Recall Issued by Central Admixture Pharmacy Services
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FDA Recalls
Philips SmartPath Device Recall for Stiffness Value Errors
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FDA Recalls
Recall of Depuy Synthes ATTUNE Revision Hinge Femoral Device
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FDA Recalls
Philips SmartPath Device Recall Over Potential Stiffness Errors
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FDA Recalls
Recall of Philips MR 7700 Upgrade
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FDA Recalls
Medline Medical Procedure Kits Recall
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FDA Recalls
Zimmer Mixing Bowl and Spatula Recall Over Packaging Seal Issues
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FDA Recalls
Recall of Medline Surgical ENT Prep Kits Due to Endotoxin Levels
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FDA Recalls
Philips Ingenia Elition S Recall Due to Potential Errors
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FDA Recalls
Recall of i-STAT EG6+ Cartridges by Abbott Point of Care Inc.
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FDA Recalls
Recall of Depuy Synthes ATTUNE Revision Hinge Femoral Product
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FDA Recalls
Medline EH Bronchoscopy Kit Recall
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FDA Recalls
Recall of Philips Evolution Upgrade 1.5T Devices
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FDA Recalls
Recall of Philips Bridge Prep Kit Due to Catheter Resistance Issue
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FDA Recalls
FDA Recall of Centurion Dermatology Shave Kits
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FDA Recalls
Recall of Centurion Medical Kits by Medline Industries
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FDA Recalls
Recall of Philips Achieva 3.0T Device
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FDA Recalls
FDA Recall of Philips Bridge Prep Kit Due to Catheter Resistance
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FDA Recalls
Recall of BD GasPak EZ Campy Pouch System for Low CO2 Levels
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FDA Recalls
Siemens epoc BGEM BUN Test Card Recall Due to Inaccurate Results
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FDA Recalls
FDA Recall of Abbott i-STAT EG7+ Cartridges Due to Inaccurate Test Results
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FDA Recalls
Recall of Immy Myco DDR Trident Neutralization Buffer Due to Contaminants
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FDA Recalls
FDA Recall of Healthmark Tip Protectors Due to Lack of Clearance
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FDA Recalls
Philips MR 7700 Device Recall Announced
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FDA Recalls
Philips Ingenia 1.5T Devices Recall Over Stiffness Value Errors
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FDA Recalls
Recall of Philips Achieva 1.5T Medical Device
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FDA Recalls
Recall of Philips Ingenia 3.0T CX Devices
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FDA Recalls high
WHILL Model F Wheelchair Recall Due to Cyber Vulnerability
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FDA Recalls
Recall of Advanced Bionics HiResolution Bionic Ear System Battery Pak
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FDA Recalls
Recall of Philips Ingenia Elition X Devices
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FDA Recalls high
FDA Recall of AIDBAGs First Aid Kits by North American Rescue LLC.
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FDA Recalls
Recall of Philips Ingenia 1.5T CX Medical Device
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FDA Recalls
Recall of Philips Achieva 1.5T Devices Due to Potential Errors
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FDA Recalls
Medline Recalls Medical Procedure Kits Due to Endotoxin Levels
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FDA Recalls
Recall of Straumann n!ce PMMA Full-arch Restoration
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FDA Recalls
Recall of Philips Ingenia Ambition S Devices
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FDA Recalls
Medline Medical Procedure Kits Recall Over Endotoxin Levels
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FDA Recalls
FDA Announces Recall of Leksell Vantage Arc System
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FDA Recalls
Recall of Medline PEDS AIRWAY PACK Kits Due to Endotoxin Levels
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FDA Recalls
Recall of i-STAT G3+ Cartridges by Abbott
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FDA Recalls
Medline Recalls Medical Procedure Kits Over Endotoxin Levels
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FDA Recalls
Philips Evolution Upgrade 3.0T Recall for Stiffness Value Errors
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FDA Recalls
Recall of Medline Centurion Medical Kits Due to Non-Sterile Alcohol Prep Pads
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FDA Recalls
Straumann n!ce Zr Dental Implant Abutments Recall
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FDA Recalls
Recall of Medline Medical Kits Containing Non-Sterile Alcohol Prep Pads
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FDA Recalls
FDA Recall of Siemens Dimension Creatinine Flex Reagent Cartridge
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FDA Recalls high
Boston Scientific Pacemaker Recall for Software Update
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