Browse Device Recalls
15 FDA medical device safety recalls.
FDA Medical Device Recall Enforcement Database
Browse 15 FDA medical device recall enforcement actions. Each entry includes the device description, reason for recall, classification (Class I through III based on severity), recalling firm, and distribution details. Use the filters below to search by year, classification, state, or keyword.
Medical Device Recalls
Browse 15 FDA device recalls.
| Date | Product | Reason | Class | Firm |
|---|---|---|---|---|
| Mar 7, 2018 | Edwards Lifesciences Femoral Venous Cannula, 20F X 55CM, resterilized. | The expiration date on the device labeling exceeds its actual validated shelf life because the st... | Class II | SPS Sterilization, Inc |
| Mar 7, 2018 | Edwards Lifesciences Aortic Perfusion Cannula, 24F x 30CM, resterilized. | The expiration date on the device labeling exceeds its actual validated shelf life because the st... | Class II | SPS Sterilization, Inc |
| Mar 7, 2018 | Edwards Lifesciences Optisite Arterial Perfusion Cannula, 22F X 24CM, resteri... | The expiration date on the device labeling exceeds its actual validated shelf life because the st... | Class II | SPS Sterilization, Inc |
| Mar 7, 2018 | Boston Scientific Wallstent RP Endoprosthesis Tracheobronchial Self-Expanding... | The expiration date on the device labeling exceeds its actual validated shelf life because the st... | Class II | SPS Sterilization, Inc |
| Mar 7, 2018 | Edwards Lifesciences Femoral Venous Cannula, 18FR, resterilized. | The expiration date on the device labeling exceeds its actual validated shelf life because the st... | Class II | SPS Sterilization, Inc |
| Mar 7, 2018 | Edwards Lifesciences EZ Glide Aortic Cannula, 24F x 37.6CM, resterilized. | The expiration date on the device labeling exceeds its actual validated shelf life because the st... | Class II | SPS Sterilization, Inc |
| Mar 7, 2018 | Boston Scientific Wallstent Endoprosthesis Tracheobronchial Self-Expanding St... | The expiration date on the device labeling exceeds its actual validated shelf life because the st... | Class II | SPS Sterilization, Inc |
| Mar 7, 2018 | Vascular Solutions Venture Rx Catheter, 6F, resterilized. | The expiration date on the device labeling exceeds its actual validated shelf life because the st... | Class II | SPS Sterilization, Inc |
| Mar 7, 2018 | Boston Scientific Wallstent RP Endoprosthesis Tracheobronchial Transhepatic B... | The expiration date on the device labeling exceeds its actual validated shelf life because the st... | Class II | SPS Sterilization, Inc |
| Mar 7, 2018 | Boston Scientific Wallstent Endoprosthesis Tracheobronchial Self-Expanding St... | The expiration date on the device labeling exceeds its actual validated shelf life because the st... | Class II | SPS Sterilization, Inc |
| Mar 7, 2018 | Boston Scientific Wallstent Enteral Endoprosthesis Colonic/Duodenal Stent, 22... | The expiration date on the device labeling exceeds its actual validated shelf life because the st... | Class II | SPS Sterilization, Inc |
| Mar 7, 2018 | Edwards Lifesciences Thin-Flex Single Stage Venous Drainage Cannula, 38FRX40C... | The expiration date on the device labeling exceeds its actual validated shelf life because the st... | Class II | SPS Sterilization, Inc |
| Mar 7, 2018 | Boston Scientific Wallstent Endoprosthesis Tracheobronchial Transhepatic Bili... | The expiration date on the device labeling exceeds its actual validated shelf life because the st... | Class II | SPS Sterilization, Inc |
| Mar 7, 2018 | Edwards Lifesciences Thin-Flex Single Stage Venous Drainage Cannula, 34F (11.... | The expiration date on the device labeling exceeds its actual validated shelf life because the st... | Class II | SPS Sterilization, Inc |
| Mar 7, 2018 | Edwards Lifesciences Avid Dual Stage Venous Drainage Cannula, 29/37F (9.6/12.... | The expiration date on the device labeling exceeds its actual validated shelf life because the st... | Class II | SPS Sterilization, Inc |
Frequently Asked Questions
When a device safety issue is identified, the manufacturer or FDA initiates a recall. The FDA publishes an enforcement report detailing the device, the reason for the recall, and distribution. Healthcare facilities and providers are notified to check their inventory and take corrective action.
All types — from simple devices like blood glucose test strips and surgical gloves to complex devices like pacemakers, defibrillators, insulin pumps, hip implants, and ventilators. Software-driven devices are increasingly common in recalls due to bugs and cybersecurity vulnerabilities.
Use the search and filter tools on this page. Each recall entry includes the device description, model numbers, and distribution details so you can determine if your device is affected. Contact your healthcare provider if you find a match.