Browse Device Recalls

4 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 4 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 4 FDA device recalls.

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DateProductReasonClassFirm
Jul 6, 2026 Brand Name: Elevaris/Spectra Medical Devices Product Name: Sodium Chloride I... Manufacturing firm, Huons, was cited for issues regarding product quality and sterility assurance... Class I Spectra Medical Devices, Llc
Jun 5, 2026 MEDLINE convenience kits labeled as: 1) TOTAL JOINT KIT, Medline Kit SKU D... Medline Industries, LP is issuing a recall for specific Medline kits containing B. Braun convenie... Class I Medline Industries, LP
Jun 5, 2026 MEDLINE convenience kits labeled as: 1) C-SECTION, Medline SKU DYNJ910835;... Medline Industries, LP is issuing a recall for specific Medline kits containing B. Braun convenie... Class I Medline Industries, LP
Jun 5, 2026 MEDLINE ANTERIOR HIP, Medline Kit SKU DYNJ909640G Medline Industries, LP is issuing a recall for specific Medline kits containing B. Braun convenie... Class I Medline Industries, LP

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.