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 10101–10120 of 38,428 recalls
Recalled Item: Hobbs Medical Spray Catheter: The Mistifier: 2.6mm 165cm Disposable For
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: 4702
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: 6548
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 Catalog Number: 6108
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: 6544
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: 4824
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: 6568
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: 6582
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 (contained in kit 6501) Catalog Number: 6541
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 and Vacu-lok Aspirating Syringe...
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: 6567
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: 4808
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 (containing 3412) Catalog Number: 6001
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 Spray Catheter: The Mistifier: 2.6mm 260cm Disposable For
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: 6562
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: 4816
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: 4704
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 Catalog Number: 6104
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 6567) Catalog Number: 6519
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: 4563-OLY
The Issue: Device label display an incorrect expiration date, extends
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.