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 6961–6980 of 38,428 recalls
Recalled Item: Compress Device Short Anchor Plug
The Issue: Anchor plugs potentially have metal burrs in the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Segmental Anchor Plug
The Issue: Anchor plugs potentially have metal burrs in the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Segmental Anchor Plug
The Issue: Anchor plugs potentially have metal burrs in the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Short Anchor Plug
The Issue: Anchor plugs potentially have metal burrs in the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Segmental Anchor Plug
The Issue: Anchor plugs potentially have metal burrs in the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Segmental Anchor Plug
The Issue: Anchor plugs potentially have metal burrs in the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Short Anchor Plug
The Issue: Anchor plugs potentially have metal burrs in the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Segmental Anchor Plug
The Issue: Anchor plugs potentially have metal burrs in the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Short Anchor Plug
The Issue: Anchor plugs potentially have metal burrs in the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Short Anchor Plug
The Issue: Anchor plugs potentially have metal burrs in the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Short Anchor Plug
The Issue: Anchor plugs potentially have metal burrs in the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Short Anchor Plug
The Issue: Anchor plugs potentially have metal burrs in the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Segmental Anchor Plug
The Issue: Anchor plugs potentially have metal burrs in the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Segmental Anchor Plug
The Issue: Anchor plugs potentially have metal burrs in the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Short Anchor Plug
The Issue: Anchor plugs potentially have metal burrs in the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Segmental Anchor Plug
The Issue: Anchor plugs potentially have metal burrs in the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT Big Bore with software version V4.8.0.10421 Model:728244 CT
The Issue: For oncology users: If the user performed off-set
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Big Bore RT with software version V4.8.0.10421- Model: 728242 CT
The Issue: For oncology users: If the user performed off-set
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectral CT on Rails
The Issue: When preparing for CCT Fluoroscopy mode and activating
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT Big Bore Oncology with software version V4.8.0.10421 Model:728243
The Issue: For oncology users: If the user performed off-set
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.