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 24761–24780 of 38,428 recalls
Recalled Item: LASEREDGE Knives
The Issue: The complaints database was reviewed and there have
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives
The Issue: The complaints database was reviewed and there have
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives
The Issue: The complaints database was reviewed and there have
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives
The Issue: The complaints database was reviewed and there have
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives
The Issue: The complaints database was reviewed and there have
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives
The Issue: The complaints database was reviewed and there have
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives
The Issue: The complaints database was reviewed and there have
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives
The Issue: The complaints database was reviewed and there have
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives
The Issue: The complaints database was reviewed and there have
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives
The Issue: The complaints database was reviewed and there have
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives
The Issue: The complaints database was reviewed and there have
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives
The Issue: The complaints database was reviewed and there have
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives
The Issue: The complaints database was reviewed and there have
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives
The Issue: The complaints database was reviewed and there have
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives
The Issue: The complaints database was reviewed and there have
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives
The Issue: The complaints database was reviewed and there have
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LASEREDGE Knives
The Issue: The complaints database was reviewed and there have
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: It is recommended for patients with weight/size between 4-22 lbs
The Issue: Product labeled as GVL 2 Stat (blades), lot
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The PreludeSYNC Radial Compression Device is a sterile
The Issue: Merit Medical Systems, Inc. announces a voluntary field
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ViperWire Advance Peripheral Guide Wire with Flex Tip
The Issue: Cardiovascular Systems, Inc. is recalling one lot of
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.