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Browse Device Recalls

3 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 3 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 3 FDA device recalls.

Clear
DateProductReasonClassFirm
Apr 9, 2021 COVID-19 Self-Test Kit *** INNOVA *** 7T Due to distributing test kits to customers who were not part of a clinical investigation. Class I INNOVA MEDICAL GROUP, INC.
Apr 9, 2021 For In Vitro Diagnostic Use Only *** 25T 888 SARS-CoV-2 Antigen *** SARS-CoV-... Due to distributing test kits to customers who were not part of a clinical investigation. Class I INNOVA MEDICAL GROUP, INC.
Apr 9, 2021 COVID-19 Self-Test Kit *** INNOVA *** 3T Due to distributing test kits to customers who were not part of a clinical investigation. Class I INNOVA MEDICAL GROUP, 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.