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 11861–11880 of 38,428 recalls
Recalled Item: Zoll
The Issue: Labeling update concerning potential leaks from the catheter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TECNIS Eyhance IOLs are permanent intraocular implants intended for implantation
The Issue: Nonconforming product was distributed in error. Product was
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll (SL-2593CO)
The Issue: Labeling update concerning potential leaks from the catheter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZOLL
The Issue: Labeling update concerning potential leaks from the catheter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll
The Issue: Labeling update concerning potential leaks from the catheter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll
The Issue: Labeling update concerning potential leaks from the catheter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll
The Issue: Labeling update concerning potential leaks from the catheter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll (IC-3893CO)
The Issue: Labeling update concerning potential leaks from the catheter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll
The Issue: Labeling update concerning potential leaks from the catheter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll
The Issue: Labeling update concerning potential leaks from the catheter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll
The Issue: Labeling update concerning potential leaks from the catheter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll
The Issue: Labeling update concerning potential leaks from the catheter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZOLL
The Issue: Labeling update concerning potential leaks from the catheter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZOLL
The Issue: Labeling update concerning potential leaks from the catheter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZOLL
The Issue: Labeling update concerning potential leaks from the catheter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll (IC-3893AE)
The Issue: Labeling update concerning potential leaks from the catheter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll
The Issue: Labeling update concerning potential leaks from the catheter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll
The Issue: Labeling update concerning potential leaks from the catheter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll
The Issue: Labeling update concerning potential leaks from the catheter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll
The Issue: Labeling update concerning potential leaks from the catheter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.