FDA Recalls, Food, Drug & Medical Device Alerts
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 1–50 of 2,262 FDA recalls. Browse by month →
FDA Recalls
Quantum 4Front 2HD Wheelchair Recall Issued
FDA ·
FDA Recalls
Quantum Rehab Q6 Edge 2.0 Wheelchair Recall
FDA ·
FDA Recalls
Stryker Strykeflow Suction/Irrigator PS Recall
FDA ·
FDA Recalls
Quantum Rehab Q6 Edge 4 Wheelchair Recall
FDA ·
FDA Recalls
COAPTIUM CONNECT Recall Issued by TISSIUM SA
FDA ·
FDA Recalls
Stryker AHTO Tube Set With Tip Packaging Recall
FDA ·
FDA Recalls
Maquet Flow Anesthesia Machines Recall
FDA ·
FDA Recalls
Philips Allura Xper Systems Recall
FDA ·
FDA Recalls
U2 Total Knee System Femoral Offset Bushing Recall
FDA ·
FDA Recalls
Boston Scientific Radial Jaw 4 Biopsy Forceps Recall
FDA ·
FDA Recalls
COAPTIUM CONNECT Recall Issued by TISSIUM SA
FDA ·
FDA Recalls
Merge OrthoPACS Recall Issued for Display Issue
FDA ·
FDA Recalls
Kingfisher Compact Individual First Aid Kit Recall
FDA ·
FDA Recalls
Aniara Diagnostica Recalls 5-PLASMA Bivalirudin Control
FDA ·
FDA Recalls
COAPTIUM CONNECT Device Recall
FDA ·
FDA Recalls
Aniara Diagnostica Recalls 5-PLASMA Bivalirudin Calibrator
FDA ·
FDA Recalls
Biomet Intramedullary Bone Saw Blade Assembly Recall
FDA ·
FDA Recalls
Quantum Q6 Edge 2.0 Wheelchair Recall
FDA ·
FDA Recalls
Stryker Single Spike Tube Set Recall Issued
FDA ·
FDA Recalls
Siemens Syva Emit Disopyramide Assay Recall
FDA ·
FDA Recalls
Philips Azurion X-Ray Systems Recall for Hard Drive Issue
FDA ·
FDA Recalls
Neuroguard IEP Carotid Stent System Recall
FDA ·
FDA Recalls
GEM Premier 7000 with iQM3 Recall Issued
FDA ·
FDA Recalls high
Halyard Convenience Kits Recall
FDA ·
FDA Recalls
Philips Allura X-Ray System Recall
FDA ·
FDA Recalls
Beckman Coulter MicroScan LabPro V5.03 Recall
FDA ·
FDA Recalls
DASH Rapid PCR Instrument Recall Issued by Nuclein LLC
FDA ·
FDA Recalls
Therabody Theragun Charger Recall Issued
FDA ·
FDA Recalls
REMISOL Advance Software Version 2.5 Recall
FDA ·
FDA Recalls
Quantum Rehab Q6 Edge 3 Wheelchair Recall
FDA ·
FDA Recalls
Quantum Rehab R-TRAK Powered Wheelchair Recall
FDA ·
FDA Recalls
Biomet Recalls Intramedullary Bone Saw Blade Assembly
FDA ·
FDA Recalls
COAPTIUM Connect Device Recall Issued
FDA ·
FDA Recalls
Hardy Diagnostics Recalls HardyDisk AST Cefiderocol (Z-2887-2026)
FDA ·
FDA Recalls
Quantum Rival Wheelchair Recall
FDA ·
FDA Recalls
Quantum Rehab Q6 Edge HD Wheelchair Recall
FDA ·
FDA Recalls
COAPTIUM CONNECT Device Recall by TISSIUM
FDA ·
FDA Recalls
Biofire Defense FilmArray NGDS Warrior Panel Recall
FDA ·
FDA Recalls high
Boston Scientific INFINION CX Lead Kits Recall
FDA ·
FDA Recalls
Quantum 1450 Powered Wheelchair Recall
FDA ·
FDA Recalls
Quantum Rehab 4Front Powered Wheelchair Recall
FDA ·
FDA Recalls
Intramedullary Bone Saw Blade Assembly Recall
FDA ·
FDA Recalls
Merge PACS Medical Imaging Workstation Recall
FDA ·
FDA Recalls
Biomet Intramedullary Bone Saw Blade Assembly Recall
FDA ·
FDA Recalls
U2 Total Knee System Femoral Valgus Offset Adaptor Recall
FDA ·
FDA Recalls
munevo DRIVE Wheelchair Control System Recall
FDA ·
FDA Recalls
Boston Scientific Radial Jaw 4 Biopsy Forceps Recall
FDA ·
FDA Recalls
COAPTIUM CONNECT Device Recall
FDA ·
FDA Recalls
Biomet Intramedullary Bone Saw Blade Assembly Recall
FDA ·
FDA Recalls
Quantum 4Front 2 Wheelchair Recall Issued
FDA ·
Download the alert category summary cited on this page: areazine-alert-category-summary.csv (CC BY 4.0). Upstream sources and cadence are documented on /methodology.