Browse Device Recalls
109 FDA medical device safety recalls.
FDA Medical Device Recall Enforcement Database
Browse 109 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 109 FDA device recalls.
| Date | Product | Reason | Class | Firm |
|---|---|---|---|---|
| Aug 25, 2014 | BioFlo PICC with ENDEXO Technology Maximal Barrier Nursing Kit, 3F-55 cm, UPN... | NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline Flush Syringes, that it ... | Class II | Navilyst Medical, Inc |
| Aug 25, 2014 | PICC Convenience Kit with Accessories, BioFlo PICC with ENDEXO and PASV Valve... | NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline Flush Syringes, that it ... | Class II | Navilyst Medical, Inc |
| Aug 25, 2014 | PICC Convenience Kit with Accessories, BioFlo PICC with ENDEXO and PASV Valve... | NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline Flush Syringes, that it ... | Class II | Navilyst Medical, Inc |
| Aug 25, 2014 | BioFlo PICC with ENDEXO Technology and PASV Valve Technology Maximal Barrier ... | NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline Flush Syringes, that it ... | Class II | Navilyst Medical, Inc |
| Aug 25, 2014 | PICC Convenience Kit with Accessories, BioFlo PICC with ENDEXO and PASV Valve... | NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline Flush Syringes, that it ... | Class II | Navilyst Medical, Inc |
| Aug 25, 2014 | BioFlo PICC with ENDEXO Technology Maximal Barrier Nursing Kit, 5F-55 cm, UPN... | NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline Flush Syringes, that it ... | Class II | Navilyst Medical, Inc |
| Aug 25, 2014 | PICC Convenience Kit with Accessories, BioFlo PICC with ENDEXO and PASV Valve... | NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline Flush Syringes, that it ... | Class II | Navilyst Medical, Inc |
| Aug 25, 2014 | PICC Convenience Kit with Accessories, BioFlo PICC with ENDEXO Technology, 5F... | NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline Flush Syringes, that it ... | Class II | Navilyst Medical, Inc |
| Nov 25, 2013 | Port Kit with Access Infusion Set under the following labels: 1) 8F/SL/Plasti... | Navilyst Medical has recalled a Port Kit with Access Infusion Set due to a possible breach of ste... | Class II | Navilyst Medical, 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.