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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
Aug 3, 2016 Medtronic EnVeo R Delivery Catheter System (DCS), Models: ENVEOR-L, ENVEOR-L-... Potential for vascular trauma with the use of the Medtronic EnVeo R Delivery Catheter System (DCS). Class II Medtronic Cardiovascular Surgery-the Heart Valv...
Jul 15, 2015 EnVeo R Loading System, Model No. LS-EnVeoR-23, LS-EnVeoR-2629, LS-EnVeoR-23-... Medtronic is recalling the EnVeo R Loading Systems because of the presence of particulate. Class I Medtronic Cardiovascular Surgery-the Heart Valv...
Aug 15, 2014 Hancock Apical Left Ventricle Connector, Model No. H174Axx, Catalog No. 0174A... Medtronic has decided to discontinue production and distribution of this low-volume product. Class II Medtronic Cardiovascular Surgery-the Heart Valv...
Jan 9, 2014 Product Name: Model 7305- Mosaic Aortic Obturator The Mosaic Aortic Obtura... Medtronic, Inc. initiated a recall of Medtronic Mosaic Aortic Obturator Model 7305 used with th... Class II Medtronic Cardiovascular Surgery-the Heart Valv...

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.