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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 27, 2021 CareStart COVID-19 Antigen Rapid Diagnostic Test for the detection of SARS-Co... Products may have been distributed to customers other than laboratories certified under the Clini... Class II Versea Diagnostics LLC
Jul 27, 2021 Healgen COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma) Qual... Products may have been distributed to customers other than laboratories certified under the Clini... Class II Versea Diagnostics LLC
Jul 27, 2021 Status COVID-19/Flu Rapid Immunoassay for Direct Detection and Differential D... Products may have been distributed to customers other than laboratories certified under the Clini... Class II Versea Diagnostics LLC
Jul 27, 2021 FaStep COVID-19 IgG/IgM Rapid Test Device Qualitative detection and differen... Products may have been distributed to customers other than laboratories certified under the Clini... Class II Versea Diagnostics 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.