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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 31, 2024 Inspire Model 4063 Stimulation Lead, component of the Inspire Upper Airway St... Labeling error with a mismatch between the shelf box serial number label and the serial number of... Class II Inspire Medical Systems Inc.
Jul 31, 2024 Inspire Model 4340 Respiratory Sensing Lead, component of the Inspire Upper A... Labeling error with a mismatch between the shelf box serial number label and the serial number of... Class II Inspire Medical Systems Inc.
May 16, 2024 Inspire Model 3028, IV Implantable Pulse Generator There is a potential manufacturing defect which can lead to electrical leakage in the sensing cir... Class I Inspire Medical Systems Inc.
Jun 12, 2018 Inspire II Model 3024 Implantable Pulse Generator (IPG) for Obstructive Sleep... Incorrect use-by date on the device registration/patient file labels. Class II Inspire Medical Systems 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.