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 18281–18300 of 38,428 recalls
Recalled Item: Drill
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Sys 2.7
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V-TEK"
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MoniTorr 10100 10-100 CSF Drainage System w/Patient Line One Way
The Issue: The firm has identified a complaint trend regarding
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CBS micro
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AURIGA XL 4007 GENERAL - DEMO SYSTEM UPN: M0068FS4007GD0 Product
The Issue: Certain Auriga consoles may exhibit faster than normal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill for 2.7mm screw
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill for 2.7mm screw
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V-TEK"
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V-TEK"
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V-TEK"
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.