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 9781–9800 of 38,428 recalls
Recalled Item: FERNO POWER X1 AMBULANCE COT- Item #0015807/UDI-DI 00190790002183 with 36V
The Issue: Batteries could become unstable when not properly maintained
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Steri-Drape
The Issue: During a recent investigation, 3M confirmed the liner
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Steri-Drape
The Issue: During a recent investigation, 3M confirmed the liner
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Steri-Drape
The Issue: During a recent investigation, 3M confirmed the liner
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Steri-Drape
The Issue: During a recent investigation, 3M confirmed the liner
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Steri-Drape
The Issue: During a recent investigation, 3M confirmed the liner
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Steri-Drape
The Issue: During a recent investigation, 3M confirmed the liner
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Steri-Drape
The Issue: During a recent investigation, 3M confirmed the liner
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Steri-Drape
The Issue: During a recent investigation, 3M confirmed the liner
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Steri-Drape
The Issue: During a recent investigation, 3M confirmed the liner
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Steri-Drape
The Issue: During a recent investigation, 3M confirmed the liner
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Steri-Drape
The Issue: During a recent investigation, 3M confirmed the liner
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Steri-Drape
The Issue: During a recent investigation, 3M confirmed the liner
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Steri-Drape
The Issue: During a recent investigation, 3M confirmed the liner
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Steri-Drape
The Issue: During a recent investigation, 3M confirmed the liner
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Steri-Drape
The Issue: During a recent investigation, 3M confirmed the liner
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Steri-Drape
The Issue: During a recent investigation, 3M confirmed the liner
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Steri-Drape
The Issue: During a recent investigation, 3M confirmed the liner
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Steri-Drape
The Issue: During a recent investigation, 3M confirmed the liner
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fogarty Arterial Embolectomy Catheters Model Number: 120602FP 120403FP...
The Issue: Due to an increase of confirmed latex deterioration
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.