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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
May 28, 2014 HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating... Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guid... Class I Nitinol Devices and Components, Inc.
May 28, 2014 HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating... Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guid... Class I Nitinol Devices and Components, Inc.
May 28, 2014 HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating... Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guid... Class I Nitinol Devices and Components, Inc.
May 28, 2014 HydroFinity Hydrophilic guidewire;Nitinol Guidewire with Hydrophilic Coating,... Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guid... Class I Nitinol Devices and Components, Inc.
May 28, 2014 HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating... Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guid... Class I Nitinol Devices and Components, Inc.
May 28, 2014 HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating... Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guid... Class I Nitinol Devices and Components, Inc.
May 28, 2014 HydroFinity Hydrophilic guidewire;Nitinol Guidewire with Hydrophilic Coating,... Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guid... Class I Nitinol Devices and Components, Inc.
May 28, 2014 HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating... Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guid... Class I Nitinol Devices and Components, Inc.
May 28, 2014 HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating... Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guid... Class I Nitinol Devices and Components, Inc.
May 28, 2014 HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating... Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guid... Class I Nitinol Devices and Components, Inc.
May 28, 2014 HydroFinity Hydrophilic guidewire; 0.035 OD, Stiff Shaft, Straight Tip, 180... Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guid... Class I Nitinol Devices and Components, Inc.
May 28, 2014 HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating... Reports of outer polymer jacket to the core wire being damaged during use on the HydroFinity Guid... Class I Nitinol Devices and Components, 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.