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Browse Device Recalls

8 FDA medical device safety recalls.

FDA Medical Device Recall Enforcement Database

Browse 8 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 8 FDA device recalls.

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DateProductReasonClassFirm
Jan 9, 2024 Signature Laparoscopic Instruments, 20mm Atraumatic Grasper with Rotating Sha... Insulation on the tube did not extend fully to the proximal end of the shaft on the instrument, l... Class II Silex Medical, LLC
Jan 9, 2024 Signature Laparoscopic Instruments, Allis Clamp Grasper with Rotating Shaft a... Insulation on the tube did not extend fully to the proximal end of the shaft on the instrument, l... Class II Silex Medical, LLC
Jan 9, 2024 Signature Laparoscopic Instruments, Alligator Grasper with Rotating Shaft and... Insulation on the tube did not extend fully to the proximal end of the shaft on the instrument, l... Class II Silex Medical, LLC
Jan 9, 2024 Signature Laparoscopic Instruments, Atraumatic Grasper with Rotating Shaft an... Insulation on the tube did not extend fully to the proximal end of the shaft on the instrument, l... Class II Silex Medical, LLC
Jan 9, 2024 Signature Laparoscopic Instruments, Dolphin Nose Grasper with Rotating Shaft ... Insulation on the tube did not extend fully to the proximal end of the shaft on the instrument, l... Class II Silex Medical, LLC
Jan 9, 2024 Signature Laparoscopic Instruments, Sharp Tooth Grasper with Rotating Shaft a... Insulation on the tube did not extend fully to the proximal end of the shaft on the instrument, l... Class II Silex Medical, LLC
Jan 9, 2024 Signature Laparoscopic Instruments, Debakey Grasper with Rotating Shaft and M... Insulation on the tube did not extend fully to the proximal end of the shaft on the instrument, l... Class II Silex Medical, LLC
Jan 9, 2024 Signature Laparoscopic Instruments, Bullet Tip Grasper with Rotating Shaft an... Insulation on the tube did not extend fully to the proximal end of the shaft on the instrument, l... Class II Silex Medical, 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.