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 30921–30940 of 38,428 recalls
Recalled Item: CROSSCHECK(R) Plating system
The Issue: The minor diameter, major diameter, thread pitch, and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CROSSCHECK(R) Plating system
The Issue: The minor diameter, major diameter, thread pitch, and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CROSSCHECK(R) Plating system
The Issue: The minor diameter, major diameter, thread pitch, and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CROSSCHECK(R) Plating system
The Issue: The minor diameter, major diameter, thread pitch, and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CROSSCHECK(R) Plating system
The Issue: The minor diameter, major diameter, thread pitch, and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CROSSCHECK(R) Plating system
The Issue: The minor diameter, major diameter, thread pitch, and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CROSSCHECK(R) Plating system
The Issue: The minor diameter, major diameter, thread pitch, and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CROSSCHECK(R) Plating system
The Issue: The minor diameter, major diameter, thread pitch, and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CROSSCHECK(R) Plating system
The Issue: The minor diameter, major diameter, thread pitch, and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CROSSCHECK(R) Plating system
The Issue: The minor diameter, major diameter, thread pitch, and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CROSSCHECK(R) Plating system
The Issue: The minor diameter, major diameter, thread pitch, and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CROSSCHECK(R) Plating system
The Issue: The minor diameter, major diameter, thread pitch, and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CROSSCHECK(R) Plating system
The Issue: The minor diameter, major diameter, thread pitch, and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CROSSCHECK(R) Plating system
The Issue: The minor diameter, major diameter, thread pitch, and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CROSSCHECK(R) Plating system
The Issue: The minor diameter, major diameter, thread pitch, and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CROSSCHECK(R) Plating system
The Issue: The minor diameter, major diameter, thread pitch, and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD FACSCalibur
The Issue: The circuit breakers on some BD FACSCalibur instruments
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: YC-1800 OPHTHALMIC YAG LASER SYSTEM
The Issue: Dear Doctor letter and Quick Reference Guide is
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge LIS software.
The Issue: There is a potential for duplicate container numbers
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Direct Water feed Kit
The Issue: The bottle assemblies were manufactured with a quality
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.