FDA Recalls, Food, Drug & Medical Device Alerts - Page 10 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 451–500 of 2,262 FDA recalls. Browse by month →
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 ·