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 19581–19600 of 38,428 recalls
Recalled Item: ORTHOFIX Catalogue Number:
The Issue: As a result of complaint investigations it was
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number:
The Issue: As a result of complaint investigations it was
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number:
The Issue: As a result of complaint investigations it was
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number:
The Issue: As a result of complaint investigations it was
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number:
The Issue: As a result of complaint investigations it was
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number:
The Issue: As a result of complaint investigations it was
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number:
The Issue: As a result of complaint investigations it was
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number:
The Issue: As a result of complaint investigations it was
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number:
The Issue: As a result of complaint investigations it was
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number:
The Issue: As a result of complaint investigations it was
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number:
The Issue: As a result of complaint investigations it was
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number:
The Issue: As a result of complaint investigations it was
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number:
The Issue: As a result of complaint investigations it was
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number:
The Issue: As a result of complaint investigations it was
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number:
The Issue: As a result of complaint investigations it was
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number:
The Issue: As a result of complaint investigations it was
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number:
The Issue: As a result of complaint investigations it was
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number:
The Issue: As a result of complaint investigations it was
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Catalogue Number:
The Issue: As a result of complaint investigations it was
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aisys Anesthesia System. Sold under the following product names: AISYS
The Issue: Upgraded Aisys anesthesia devices and Aisys CS2 anesthesia
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.