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 28981–29000 of 38,428 recalls
Recalled Item: Philips Allura Xper FD20 Ceiling version only
The Issue: Normally, movement of the C-arc is initially stopped
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD OR Table
The Issue: Normally, movement of the C-arc is initially stopped
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10
The Issue: The use of Allura Xper, Allura Clarity, Allura
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS V3000
The Issue: The use of Allura Xper, Allura Clarity, Allura
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10/10
The Issue: The use of Allura Xper, Allura Clarity, Allura
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS CV
The Issue: The use of Allura Xper, Allura Clarity, Allura
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/10
The Issue: The use of Allura Xper, Allura Clarity, Allura
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20/20 OR Table
The Issue: The use of Allura Xper, Allura Clarity, Allura
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS Allura 15-12 (biplane)
The Issue: The use of Allura Xper, Allura Clarity, Allura
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10 OR Table
The Issue: The use of Allura Xper, Allura Clarity, Allura
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS H5000
The Issue: The use of Allura Xper, Allura Clarity, Allura
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD20 Biplane
The Issue: The use of Allura Xper, Allura Clarity, Allura
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS BH3000
The Issue: The use of Allura Xper, Allura Clarity, Allura
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS BH5000
The Issue: The use of Allura Xper, Allura Clarity, Allura
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS BV5000: Model Number: 72249 The Philips INTEGRIS 3000 I
The Issue: The use of Allura Xper, Allura Clarity, Allura
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura CV20
The Issue: The use of Allura Xper, Allura Clarity, Allura
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS Allura 15-12 (mono)
The Issue: The use of Allura Xper, Allura Clarity, Allura
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS H3000
The Issue: The use of Allura Xper, Allura Clarity, Allura
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS BN/BV3000
The Issue: The use of Allura Xper, Allura Clarity, Allura
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UNIQ FD
The Issue: The use of Allura Xper, Allura Clarity, Allura
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.