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Browse Device Recalls

12 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 12 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 12 FDA device recalls.

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DateProductReasonClassFirm
Dec 28, 2016 Intact Disposable Wands (part of the Intact System) 777-112: 5 Pack 12mm Dis... Product sterility compromised due to breach of sterile barrier Class II Medtronic Advanced Energy, LLC
Dec 28, 2016 Intact Disposable Wands (part of the Intact System) 777-120: 5 Pack 20mm Dis... Product sterility compromised due to breach of sterile barrier Class II Medtronic Advanced Energy, LLC
Dec 28, 2016 Intact Disposable Wands (part of the Intact System) 900-130: 5 Pack 30mm Dis... Product sterility compromised due to breach of sterile barrier Class II Medtronic Advanced Energy, LLC
Dec 28, 2016 Intact Disposable Wands (part of the Intact System) 900-120: 5 Pack 20mm Dis... Product sterility compromised due to breach of sterile barrier Class II Medtronic Advanced Energy, LLC
Dec 28, 2016 Intact Disposable Wands (part of the Intact System) 900-112: 5 Pack 12mm Dis... Product sterility compromised due to breach of sterile barrier Class II Medtronic Advanced Energy, LLC
Dec 28, 2016 Intact Disposable Wands (part of the Intact System) 777-120BT: 5 Pack 20mm D... Product sterility compromised due to breach of sterile barrier Class II Medtronic Advanced Energy, LLC
Dec 28, 2016 Intact Disposable Wands (part of the Intact System) 777-110: 5 Pack 10mm Dis... Product sterility compromised due to breach of sterile barrier Class II Medtronic Advanced Energy, LLC
Dec 28, 2016 Intact Disposable Wands (part of the Intact System) 900-115: 5 Pack 15mm Dis... Product sterility compromised due to breach of sterile barrier Class II Medtronic Advanced Energy, LLC
Dec 28, 2016 Intact Disposable Wands (part of the Intact System) 777-115BT: 5 Pack 15mm D... Product sterility compromised due to breach of sterile barrier Class II Medtronic Advanced Energy, LLC
Dec 28, 2016 Intact Disposable Wands (part of the Intact System) 777-112BT: 5 Pack 12mm D... Product sterility compromised due to breach of sterile barrier Class II Medtronic Advanced Energy, LLC
Dec 28, 2016 Intact Disposable Wands (part of the Intact System) 777-115: 5 Pack 15mm Dis... Product sterility compromised due to breach of sterile barrier Class II Medtronic Advanced Energy, LLC
Nov 12, 2013 Medtronic Advanced Energy Aquamantys3 Pump Generator; Product Catalog Number:... The internal protection circuitry on the electrosurgical output that prevents a patient from expo... Class II Medtronic Advanced Energy, 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.