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 2941–2960 of 38,428 recalls
Recalled Item: Allura Xper FD20 Biplane
The Issue: Possibility of the patient falling from the table
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 3 M15
The Issue: Possibility of the patient falling from the table
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura CV20
The Issue: Possibility of the patient falling from the table
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 M20
The Issue: Possibility of the patient falling from the table
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 3 M12
The Issue: Possibility of the patient falling from the table
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20
The Issue: Possibility of the patient falling from the table
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20 Biplane OR Table
The Issue: Possibility of the patient falling from the table
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/15
The Issue: Possibility of the patient falling from the table
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 5 M12
The Issue: Possibility of the patient falling from the table
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20 OR Table
The Issue: Possibility of the patient falling from the table
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 7 M12
The Issue: Possibility of the patient falling from the table
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/10
The Issue: Possibility of the patient falling from the table
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10 - Catalog numbers: (1) 722003
The Issue: Possibility of the patient falling from the table
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10C
The Issue: Possibility of the patient falling from the table
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardio Vascular-Allura Centron
The Issue: Possibility of the patient falling from the table
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/20
The Issue: Possibility of the patient falling from the table
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 5 M20
The Issue: Possibility of the patient falling from the table
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10/10
The Issue: Possibility of the patient falling from the table
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura CV20 System Code: 722031
The Issue: safety issue with the AD7 and AD7X
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion 3 M12 System Code: (1) 722063 (2) 722221
The Issue: safety issue with the AD7 and AD7X
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.