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 31561–31580 of 38,428 recalls
Recalled Item: PKG
The Issue: The parameters provided in the Laparoscopic Manual Instruments
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG
The Issue: The parameters provided in the Laparoscopic Manual Instruments
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG
The Issue: The parameters provided in the Laparoscopic Manual Instruments
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG
The Issue: The parameters provided in the Laparoscopic Manual Instruments
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG
The Issue: The parameters provided in the Laparoscopic Manual Instruments
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG
The Issue: The parameters provided in the Laparoscopic Manual Instruments
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG
The Issue: Stryker Endoscopy is recalling Laparoscopic manual instruments and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG
The Issue: The parameters provided in the Laparoscopic Manual Instruments
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG
The Issue: The parameters provided in the Laparoscopic Manual Instruments
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG
The Issue: The parameters provided in the Laparoscopic Manual Instruments
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG
The Issue: The parameters provided in the Laparoscopic Manual Instruments
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG
The Issue: The parameters provided in the Laparoscopic Manual Instruments
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG
The Issue: The parameters provided in the Laparoscopic Manual Instruments
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG
The Issue: The parameters provided in the Laparoscopic Manual Instruments
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG
The Issue: The parameters provided in the Laparoscopic Manual Instruments
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG
The Issue: The parameters provided in the Laparoscopic Manual Instruments
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG
The Issue: The parameters provided in the Laparoscopic Manual Instruments
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG
The Issue: The parameters provided in the Laparoscopic Manual Instruments
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG
The Issue: The parameters provided in the Laparoscopic Manual Instruments
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PKG
The Issue: The parameters provided in the Laparoscopic Manual Instruments
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.