Browse Device Recalls

5 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 5 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 5 FDA device recalls.

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DateProductReasonClassFirm
Dec 23, 2024 AnchorFast Guard, Oral Endotracheal Tube Fastener, REF 9800, Hollister received reports of decreased skin barrier wear time which could can lead to tube migra... Class II Hollister Incorporated
Dec 23, 2024 AnchorFast Guard Select, Oral Endotracheal Tube Fastener, REF 9700, Hollister received reports of decreased skin barrier wear time which could can lead to tube migra... Class II Hollister Incorporated
Dec 23, 2024 AnchorFast, Oral Endotracheal Tube Fastener, REF 9799, Hollister received reports of decreased skin barrier wear time which could can lead to tube migra... Class II Hollister Incorporated
Dec 23, 2024 AnchorFast SlimFit, Oral Endotracheal Tube Fastener, REF 9787, Hollister received reports of decreased skin barrier wear time which could can lead to tube migra... Class II Hollister Incorporated
Feb 11, 2021 Vertical Drain Tube Attachment Device (VTAD) (Gastrointestinal tube and acces... The tube holder can separate from the barrier that secures the device to the patients' body. The... Class II Hollister Incorporated

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.