FDA Recalls, Food, Drug & Medical Device Alerts - Page 6 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 251–300 of 2,262 FDA recalls. Browse by month →
FDA Recalls high
Abiomed Intro Kit Recall Due to Sheath Leakage Risk
FDA ·
FDA Recalls high
Abiomed Impella 5.5 Smart Assist Set Recall
FDA ·
FDA Recalls high
Abiomed Introducer Kit for Impella Recall
FDA ·
FDA Recalls high
Abiomed Impella CP Set Recall Issued
FDA ·
FDA Recalls
3B Medical Recalls Rio II Nasal Pillows Interface
FDA ·
FDA Recalls high
Abiomed Impella RP Flex Recall Due to Sheath Leakage
FDA ·
FDA Recalls
Medtronic DLP One-Piece Pediatric Arterial Cannula Recall
FDA ·
FDA Recalls
da Vinci SP Instrument Arm Drape Recall
FDA ·
FDA Recalls
Medline TOTAL KNEE PACK-LF Kits Recall
FDA ·
FDA Recalls
Olympus Toomey Evacuator 50cc Recall Issued
FDA ·
FDA Recalls
Orthofix MINIRAIL External Fixation Device Recall
FDA ·
FDA Recalls
Optima XR240amx Mobile Digital Radiographic System Recall
FDA ·
FDA Recalls
Vasoview Hemopro 2 Endoscopic Vessel Harvesting System Recall
FDA ·
FDA Recalls high
Abiomed Impella 5.5 SmartAssist S2 Set Recall
FDA ·
FDA Recalls high
Argon Medical Devices Recalls T-Lok Bone Marrow Trays
FDA ·
FDA Recalls
Medtronic Bio-Medicus Adult Cannula Kit Recall
FDA ·
FDA Recalls high
Abiomed Impella CP Introducer Kit Recall
FDA ·
FDA Recalls
Orthofix MINIRAIL Fixator Recall Issued Over Labeling Error
FDA ·
FDA Recalls high
Abiomed Impella CP Set Recall Due to Sheath Leakage
FDA ·
FDA Recalls
Medline TOTAL KNEE PACK Recall
FDA ·
FDA Recalls
Orthofix Articulated Minirail Fixator Recall Due to Labeling Error
FDA ·
FDA Recalls high
Argon Medical Devices Recalls One-Piece Introducer Tray
FDA ·
FDA Recalls
ICU Medical Plum Solo Precision IV Pump Recall
FDA ·
FDA Recalls high
Abiomed Introducer Kit for Impella Recall
FDA ·
FDA Recalls high
Argon Medical Devices Recalls Transvenous Pacing Electrode Trays
FDA ·
FDA Recalls high
Abiomed Insertion Kit Recall Due to Sheath Leakage
FDA ·
FDA Recalls
Daavlin Photera 600 Phototherapy Device Recall
FDA ·
FDA Recalls high
Argon Medical Devices Recalls Arterial Line Kit
FDA ·
FDA Recalls
Olympus Glass Body for 194 Ellik Evacuator Recall
FDA ·
FDA Recalls
Olympus Toomey Evacuator Recalled Over Sterilization Issue
FDA ·
FDA Recalls
Tosoh Bioscience Recalls ST AIA-Pack Testosterone
FDA ·
FDA Recalls high
Argon Medical Devices Recalls General Biospy Tray
FDA ·
FDA Recalls
Optima XR220amx Mobile Radiographic System Recall
FDA ·
FDA Recalls
Photera 400 Phototherapy Device Recall
FDA ·
FDA Recalls high
Abiomed Introducer Kit for Impella Recall
FDA ·
FDA Recalls
Olympus Ellik Evacuator Recall Issued
FDA ·
FDA Recalls high
Abiomed Impella CP Introducer Kit Recall
FDA ·
FDA Recalls
Optima XR200amx Recall Issued by GE Medical Systems
FDA ·
FDA Recalls
Photera 600 3-D Phototherapy Device Recall
FDA ·
FDA Recalls
ICU Medical Plum Duo Infusion Pump Recall
FDA ·
FDA Recalls high
Abiomed Impella CP Introducer Kit Recall
FDA ·
FDA Recalls
Papablic Replacement Brush Heads Recall
FDA ·
FDA Recalls
Papablic Replacement Brush Heads Recall
FDA ·
FDA Recalls high
Abiomed Impella CP Set Recall Due to Leakage Risk
FDA ·
FDA Recalls
Boston Scientific Rapid Refill Continuous Injection System Recall
FDA ·
FDA Recalls
Orthofix MINIRAIL External Fixation Device Recall
FDA ·
FDA Recalls high
D'Dioses Guayaba Ice Pop Recall
FDA ·
FDA Recalls
Pillsbury Kaiser Roll Dough Recall for Potential Glass
FDA ·
FDA Recalls
Pillsbury Bread Rolls Recall Due to Potential Glass
FDA ·
FDA Recalls high
D'Dioses Rompope Ice Pop Recall for Undeclared Allergens
FDA ·