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 21361–21380 of 38,428 recalls
Recalled Item: Box Plate
The Issue: Firm is conducting a voluntary recall of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rival Reduce Kit Locking and Non-Locking Screw D 2.0MM
The Issue: Firm is conducting a voluntary recall of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Y-Plate
The Issue: Firm is conducting a voluntary recall of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L-Plate
The Issue: Firm is conducting a voluntary recall of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rival View Kit Locking and Non-Locking Screw D 2.7MM
The Issue: Firm is conducting a voluntary recall of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lapidus Plate
The Issue: Firm is conducting a voluntary recall of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CC Plate
The Issue: Firm is conducting a voluntary recall of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MTP Plate
The Issue: Firm is conducting a voluntary recall of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-Locking Screw
The Issue: Firm is conducting a voluntary recall of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Locking Screw
The Issue: Firm is conducting a voluntary recall of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-Locking Screw
The Issue: Firm is conducting a voluntary recall of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-Locking Screw
The Issue: Firm is conducting a voluntary recall of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Locking Screw
The Issue: Firm is conducting a voluntary recall of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H-Plate
The Issue: Firm is conducting a voluntary recall of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Evans Plate
The Issue: Firm is conducting a voluntary recall of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Locking Screw
The Issue: Firm is conducting a voluntary recall of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rival Reduce Kit Plates
The Issue: Firm is conducting a voluntary recall of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyTouch (ET) Insulin Syringe 29G 1ml ¿" (Item 829155) Product
The Issue: The retail shelf cartons may be labeled with
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EasyTouch (ET) Insulin Syringe 29G 0.5ml ¿" (Item 829555) Product
The Issue: The retail shelf cartons may be labeled with
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Visaris Vision/Auto
The Issue: A failure of the tube arm suspension is
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.