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 10081–10100 of 38,428 recalls
Recalled Item: The product is a handheld ultraviolet-C germicidal wand and contains two
The Issue: Excessive ultraviolet-C radiation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number: 6028
The Issue: Device label display an incorrect expiration date, extends
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freeman Pancreatic Flexi-Stent Kits: Single Pigtail Catalog Number: 6501
The Issue: Device label display an incorrect expiration date, extends
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Medical Polypectomy Snare Catalog Number: 4575-OLY
The Issue: Device label display an incorrect expiration date, extends
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freeman Pancreatic Flexi-Stent Kit (containing 6533) Catalog Number: 6507
The Issue: Device label display an incorrect expiration date, extends
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Transbronchial Aspiration Needle Catalog Number: 4621
The Issue: Device label display an incorrect expiration date, extends
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Posi-Stop Injection Needle Catalog Number: 4722
The Issue: Device label display an incorrect expiration date, extends
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Medical Grasping Forceps Catalog Number:5004
The Issue: Device label display an incorrect expiration date, extends
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Medical Polypectomy Snare Catalog Number: 4565-OLY
The Issue: Device label display an incorrect expiration date, extends
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freeman Pancreatic Flexi-Stent Kit (containing 6568) Catalog Number: 6529
The Issue: Device label display an incorrect expiration date, extends
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Biliary Pigtail Stent Kits (contains 3412) Catalog Number: 6027
The Issue: Device label display an incorrect expiration date, extends
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Medical Cytology Brush Catalog Number: 4204
The Issue: Device label display an incorrect expiration date, extends
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freeman Pancreatic Flexi-Stent Catalog Number: 6533
The Issue: Device label display an incorrect expiration date, extends
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Helical Retrieval Basket Catalog Number: 4822
The Issue: Device label display an incorrect expiration date, extends
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Medical Cytology Brush Catalog Number: 4206
The Issue: Device label display an incorrect expiration date, extends
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Helical Retrieval Basket Catalog Number: 4832
The Issue: Device label display an incorrect expiration date, extends
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freeman Pancreatic Flexi-Stent Kit (containing 6352) Catalog Number: 6321
The Issue: Device label display an incorrect expiration date, extends
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Freeman Pancreatic Flexi-Stent Catalog Number: 6584
The Issue: Device label display an incorrect expiration date, extends
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Helical Retrieval Basket Catalog Number: 4806
The Issue: Device label display an incorrect expiration date, extends
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Posi-Stop Injection Needle Catalog Number: 4718
The Issue: Device label display an incorrect expiration date, extends
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.