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 18301–18320 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: MaxiCan 4.5 countersink
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
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 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: AURIGA 30 GENERAL - DEMO SYSTEM UPN: M0068S30GD0 Product Usage:
The Issue: Certain Auriga consoles may exhibit faster than normal
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: CBS high
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CBS high
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: 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 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: Drill for 3.5mm screw
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 - ZERO COST SYSTE UPN: FS4007GZ0
The Issue: Certain Auriga consoles may exhibit faster than normal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CBS 4.0 countersink
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.