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 28081–28100 of 38,428 recalls
Recalled Item: Olympus
The Issue: If excessive pressure is applied to the distal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus
The Issue: If excessive pressure is applied to the distal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus
The Issue: If excessive pressure is applied to the distal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus
The Issue: If excessive pressure is applied to the distal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus
The Issue: If excessive pressure is applied to the distal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus
The Issue: If excessive pressure is applied to the distal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus
The Issue: If excessive pressure is applied to the distal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus
The Issue: If excessive pressure is applied to the distal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus
The Issue: If excessive pressure is applied to the distal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus
The Issue: If excessive pressure is applied to the distal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus
The Issue: If excessive pressure is applied to the distal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hill-Rom Bariatric Power Recliner
The Issue: The recliners were shipped without the foot rest
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus
The Issue: If excessive pressure is applied to the distal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus
The Issue: If excessive pressure is applied to the distal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus
The Issue: If excessive pressure is applied to the distal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeaterBaum Foot & Ankle Heating Pad
The Issue: Products are marketed without a cleared 510k
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI H/S Cuvette
The Issue: The CDI System 500 monitor displays the "H/S
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Convenience Kits from Centurion that contain an In-Vision- Plus Needleless
The Issue: Convenience Kits contain an In-Vision-Plus Needleless IV Connector,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Patient transport Shuttle with Trendelenburg quick adjustment function (Jupiter
The Issue: Complaints were received of the table top on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V-Twin
The Issue: Instrument stopped working due to a software lockup,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.