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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