Medical Device Recalls
This is our largest category by volume. The FDA tracks recalls for an enormous range of medical devices: implants, pacemakers, insulin pumps, surgical tools, blood glucose monitors, X-ray machines, prosthetics, contact lenses, and home health equipment, among many others. We have records dating back to 2005 and add new ones as the FDA publishes them.
Device recalls can happen because of software bugs, manufacturing defects, bacterial contamination, incorrect labeling, or design flaws that lead to inaccurate results or equipment failure. Class I recalls are the most serious and mean the device could cause injury or death.
Showing 3661–3680 of 38,428 recalls
Recalled Item: Stryker Neptune SafeAir Rocker-Switch Smoke Evacuation Pencil
The Issue: There is a potential for the product to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Neptune SafeAir Smoke Evacuation Pencil Coated Rocker-Switch
The Issue: There is a potential for the product to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARROLLTON HIP FX Convenience kit used for surgical procedures
The Issue: Products within a Medline pack may be impacted
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Neptune SafeAir Smoke Evacuation Pencil
The Issue: There is a potential for the product to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Neptune SafeAir Smoke Evacuation Pencil Coated Push-Button
The Issue: There is a potential for the product to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTHROSCOPY Convenience kit used for surgical procedures
The Issue: Products within a Medline pack may be impacted
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: microTargeting Insertion Tube Set
The Issue: A complaint was received (MDR 3002250546-2024-00003) prompting an
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEERA CL mobile operating table - Designed for the placement
The Issue: Error code "50037" occurs on the IR-Hand Control
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEERA CL mobile operating table - Designed for the placement
The Issue: Error code "50037" occurs on the IR-Hand Control
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEERA CL mobile operating table - Designed for the placement
The Issue: Error code "50037" occurs on the IR-Hand Control
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEERA CL mobile operating table - Designed for the placement
The Issue: Error code "50037" occurs on the IR-Hand Control
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEERA CL mobile operating table - Designed for the placement
The Issue: Error code "50037" occurs on the IR-Hand Control
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEERA CL mobile operating table - Designed for the placement
The Issue: Error code "50037" occurs on the IR-Hand Control
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal CHILDREN'S LAPTRACEPACK
The Issue: DeRoyal is recalling certain lots of surgical procedure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEERA CL mobile operating table - Designed for the placement
The Issue: Error code "50037" occurs on the IR-Hand Control
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEERA CL mobile operating table - Designed for the placement
The Issue: Error code "50037" occurs on the IR-Hand Control
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal CHILDREN'S ORTHOPEDIC TRACEPACK
The Issue: DeRoyal is recalling certain lots of surgical procedure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal CHILDREN'S GENERAL TRACEPACK
The Issue: DeRoyal is recalling certain lots of surgical procedure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Centricity Universal Viewer Zero Footprint
The Issue: GE HealthCare has become aware of an issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DeRoyal C-SECTION TRACEPACK
The Issue: DeRoyal is recalling certain lots of surgical procedure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.