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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