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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
Feb 2, 2017 Elcam Minimal Residual Volume Luer-activated Swabable-stockcock (MRVLS) 4w gx... The stopcock was found to have punctures. Class II Elcam Medical, Inc.
Jul 19, 2015 Elcam Medical Minimal Residual Volume Luer activated Swabbable stopcock (MRVL... Punctured blister packages were detected during the packaging process at the manufacturing site. ... Class II Elcam Medical, Inc.
Jul 19, 2015 Elcam Medical MANI 3G Plate BLS RAD B.BRAUN; Manifold for pressure monitoring... Punctured blister packages were detected during the packaging process at the manufacturing site. ... Class II Elcam Medical, 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.