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Browse Device Recalls

13 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 13 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 13 FDA device recalls.

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DateProductReasonClassFirm
Jun 15, 2020 POWERWAND XL 4Fr 8cm Maximum Barrier Kit (Introducer with an Extended Dwell C... Convenience kit mislabeled with the incorrect catheter effective length on the device label and t... Class III Access Scientific LLC
Apr 23, 2020 BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND XL 4Fr 10cm Max ... Saline Flush Syringe compromised sterility due to holes in the packaging. Class II Access Scientific LLC
Apr 23, 2020 BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND XL 3Fr 6cm Quick... Saline Flush Syringe compromised sterility due to holes in the packaging. Class II Access Scientific LLC
Apr 23, 2020 BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND XL 4Fr 8cm Max B... Saline Flush Syringe compromised sterility due to holes in the packaging. Class II Access Scientific LLC
Apr 23, 2020 BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND XL 4Fr 8cm Quick... Saline Flush Syringe compromised sterility due to holes in the packaging. Class II Access Scientific LLC
Apr 23, 2020 BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND XL 4Fr 10cm Quic... Saline Flush Syringe compromised sterility due to holes in the packaging. Class II Access Scientific LLC
Apr 23, 2020 BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND" ED Quick Kit 3F... Saline Flush Syringe compromised sterility due to holes in the packaging. Class II Access Scientific LLC
Apr 23, 2020 BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND XL 5Fr 8cm Quick... Saline Flush Syringe compromised sterility due to holes in the packaging. Class II Access Scientific LLC
Apr 23, 2020 BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND XL 4Fr 10cm Exte... Saline Flush Syringe compromised sterility due to holes in the packaging. Class II Access Scientific LLC
Apr 23, 2020 BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND XL 5Fr 10cm Quic... Saline Flush Syringe compromised sterility due to holes in the packaging. Class II Access Scientific LLC
Apr 23, 2020 BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND"XL Alternate Sit... Saline Flush Syringe compromised sterility due to holes in the packaging. Class II Access Scientific LLC
Apr 23, 2020 BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND XL 3Fr 6cm Pedia... Saline Flush Syringe compromised sterility due to holes in the packaging. Class II Access Scientific LLC
Apr 23, 2020 BD PosiFlush SF Saline Flush Syringe 10 mL used in POWERWAND XL 5Fr 8cm Max B... Saline Flush Syringe compromised sterility due to holes in the packaging. Class II Access Scientific LLC

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.