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 31261–31280 of 38,428 recalls
Recalled Item: NAMIC Convenience Kit
The Issue: The labelled expiration dating of the affected product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit
The Issue: The labelled expiration dating of the affected product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit
The Issue: The labelled expiration dating of the affected product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit
The Issue: The labelled expiration dating of the affected product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit
The Issue: The labelled expiration dating of the affected product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit
The Issue: The labelled expiration dating of the affected product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit
The Issue: The labelled expiration dating of the affected product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit
The Issue: The labelled expiration dating of the affected product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit
The Issue: The labelled expiration dating of the affected product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit
The Issue: The labelled expiration dating of the affected product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit
The Issue: The labelled expiration dating of the affected product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit
The Issue: The labelled expiration dating of the affected product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit
The Issue: The labelled expiration dating of the affected product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit
The Issue: The labelled expiration dating of the affected product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit
The Issue: The labelled expiration dating of the affected product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit
The Issue: The labelled expiration dating of the affected product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NAMIC Convenience Kit
The Issue: The labelled expiration dating of the affected product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mallory Head 4 Finned Acetabular Shell 50 mm
The Issue: Biomet recalled the Mallory Head 4 Finned Acetabular
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ringloc+ Acetabular Shell Finned 52 mm
The Issue: Biomet recalled the Mallory Head 4 Finned Acetabular
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alive ECG App 2.1.2 ( a medical device application for
The Issue: Alive ECG App version 2.1.2 (intended to be
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.