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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.

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DateProductReasonClassFirm
Oct 13, 2025 TMJ Bilateral Implant REF: CHG020 Sterile EO, Rx Only Patient-fitted temporomandibular joint implant contained discrepancy in screw hole position. Class I TMJ Solutions Inc
Jul 24, 2024 Stryker TMJ Unilateral Implant, REF: GHG010, consisting of the following com... Patient-fitted temporomandibular (TMJ) prothesis contained incorrect components, SterileEO Class II TMJ Solutions Inc
Mar 12, 2018 Patient-Fitted Temporomandibular (TMJ) Right Mandibular Component part of TM... This device was mislabeled and is not the correct component for this patient. Class II TMJ Solutions 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.