FDA Recalls, Food, Drug & Medical Device Alerts - Page 28 of 46

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 1,351–1,400 of 2,262 FDA recalls. Browse by month →

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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FDA Recalls

Philips Ingenia 3.0T Device Recall Announced

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FDA Recalls

Medline Cervical Pack Recall Due to Endotoxin Levels

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FDA Recalls

Medline Spinal Fusion Kit Recall

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FDA Recalls

Recall of VACUUM BAG SU LARGE Specimen Container by Milestone S.R.L.

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FDA Recalls

Medline Medical Kits Recall Due to Non-Sterile Alcohol Prep Pads

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FDA Recalls

Medline Robotic Hysterectomy Kits Recall Over Endotoxin Levels

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FDA Recalls

Recall of Philips SmartPath to Ingenia Elition X Devices

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FDA Recalls

Medline Kits Recall Due to Non-Sterile Alcohol Prep Pads

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FDA Recalls

Recall of Medline Microdiscectomy Packs Due to Endotoxin Levels

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FDA Recalls

Medline ANGIO PACK-LF Recall Over Endotoxin Levels

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FDA Recalls

Medline SPINE PACK-LF Kit Recall

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FDA Recalls high

WHILL Model C2 Wheelchair Recall Over Cyber Vulnerability

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FDA Recalls

FDA Recall of Medline Medical Kits Due to Non-Sterile Alcohol Prep Pads

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FDA Recalls high

Boston Scientific CRT Devices Recall

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FDA Recalls

Recall of Philips SmartPath to dStream Device

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FDA Recalls

FDA Recall of Genius Review Station Display

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FDA Recalls

Medline Medical Procedure Kits Recall

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FDA Recalls

Recall of BD GasPak EZ CO2 Pouch System Due to Low Carbon Dioxide Levels

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FDA Recalls high

Enoki Mushroom Recall by HEMU TRADING INC

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FDA Recalls

Recall of KLG Kesar Mukhwas by Ganesha Enterprises

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FDA Recalls

Recall of Calypso Tropic Tango Lemonade Due to Undeclared Yellow No. 5

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FDA Recalls

FDA Recall of My Mochi Strawberry Non-Dairy Frozen Dessert Due to Foreign Object

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FDA Recalls

Recall of 52USA Popping Boba Strawberry Flavor

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FDA Recalls

Recall of Einstein Bros. Bagels Honey Almond Shmear Due to Undeclared Allergen

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FDA Recalls

Recall of Specially SELECTED Vanilla Creme Brulee Due to Possible Glass Contamination

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FDA Recalls

FDA Recall of 52USA Popping Boba Mango Flavor Over Unapproved Colors

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FDA Recalls

FDA Recall of 52USA Popping Boba Due to Unapproved Colors

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FDA Recalls

FDA Recall of Negita Cracker- Shrimp Due to Undeclared Ingredient

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FDA Recalls

Recall of fentaNYL Citrate Injectable Solution by Wells Pharma

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FDA Recalls

Recall of Levocarnitine Injection by American Regent

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FDA Recalls

FDA Recall of Phenylephrine Hydrochloride Injectable Solution by Wells Pharma

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FDA Recalls

Systane Eye Gel Recall Due to Sterility Concerns

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FDA Recalls

FDA Recall of Lidocaine Wound Gel Due to Failed pH Specifications

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FDA Recalls

FDA Recall of fentaNYL Citrate Injectable Solution by Wells Pharma

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FDA Recalls

FDA Recall of Optase Dry Eye Intense Drops Due to Sterility Concerns

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FDA Recalls

Recall of Alendronate Sodium Oral Solution by Hikma Pharmaceuticals

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FDA Recalls

GenTeal Tears Eye Gel Recall Due to Sterility Concerns

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FDA Recalls

iVIZIA Dry Eye Recall Over Sterility Issues

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FDA Recalls

Recall of Ketamine Hydrochloride Injectable Solution by Wells Pharma

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