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 5041–5060 of 38,428 recalls
Recalled Item: ADVANTA VXT
The Issue: Complaints of reported separation of the Slider GDS
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLIXENE
The Issue: Complaints of reported separation of the Slider GDS
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLIXENE
The Issue: Complaints of reported separation of the Slider GDS
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HA FlexTrak-Patient transport functionality to transport the patient from the
The Issue: Oil may leak from the HA FlexTrack Trolley
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLIXENE
The Issue: Complaints of reported separation of the Slider GDS
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT
The Issue: Complaints of reported separation of the Slider GDS
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLIXENE
The Issue: Complaints of reported separation of the Slider GDS
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLIXENE
The Issue: Complaints of reported separation of the Slider GDS
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT
The Issue: Complaints of reported separation of the Slider GDS
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLIXENE
The Issue: Complaints of reported separation of the Slider GDS
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT
The Issue: Complaints of reported separation of the Slider GDS
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT
The Issue: Complaints of reported separation of the Slider GDS
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT
The Issue: Complaints of reported separation of the Slider GDS
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT
The Issue: Complaints of reported separation of the Slider GDS
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLIXENE
The Issue: Complaints of reported separation of the Slider GDS
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT
The Issue: Complaints of reported separation of the Slider GDS
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT
The Issue: Complaints of reported separation of the Slider GDS
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLIXENE
The Issue: Complaints of reported separation of the Slider GDS
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT
The Issue: Complaints of reported separation of the Slider GDS
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANTA VXT
The Issue: Complaints of reported separation of the Slider GDS
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.