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.

38,428 total recalls
0 this month

Showing 10121–10140 of 38,428 recalls

July 29, 2022· Hobbs Medical, Inc.

Recalled Item: Freeman Pancreatic Flexi-Stent Kit (containing 6566) Catalog Number: 6518

The Issue: Device label display an incorrect expiration date, extends

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
July 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Medical Grasping Forceps Catalog Number: 5008

The Issue: Device label display an incorrect expiration date, extends

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
July 29, 2022· Hobbs Medical, Inc.

Recalled Item: Freeman Pancreatic Flexi-Stent Catalog Number: 6534

The Issue: Device label display an incorrect expiration date, extends

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
July 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Helical Retrieval Basket Catalog Number: 4830

The Issue: Device label display an incorrect expiration date, extends

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
July 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Retrieval Forceps Catalog Number: 5018

The Issue: Device label display an incorrect expiration date, extends

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
July 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Medical Polypectomy Snare Catalog Number: 4564

The Issue: Device label display an incorrect expiration date, extends

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
July 29, 2022· Hobbs Medical, Inc.

Recalled Item: Freeman Pancreatic Flexi-Stent Kit Catalog Number: 6352

The Issue: Device label display an incorrect expiration date, extends

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
July 29, 2022· Hobbs Medical, Inc.

Recalled Item: Freeman Pancreatic Flexi-Stent Kit Catalog Number: 6351

The Issue: Device label display an incorrect expiration date, extends

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
July 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number:6004

The Issue: Device label display an incorrect expiration date, extends

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
July 29, 2022· Hobbs Medical, Inc.

Recalled Item: Freeman Pancreatic Flexi-Stent Catalog Number: 6535

The Issue: Device label display an incorrect expiration date, extends

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
July 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Scope Introducer Catalog Number: 4650

The Issue: Device label display an incorrect expiration date, extends

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
July 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Medical Polypectomy Snare Catalog Number: 7202

The Issue: Device label display an incorrect expiration date, extends

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
July 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number: 6024

The Issue: Device label display an incorrect expiration date, extends

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
July 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Helical Retrieval Basket Catalog Number: 4814

The Issue: Device label display an incorrect expiration date, extends

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
July 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Biliary Pigtail Stent Kits Catalog Number: 6105

The Issue: Device label display an incorrect expiration date, extends

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
July 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Posi-Stop Injection Needle Catalog Number: 4720

The Issue: Device label display an incorrect expiration date, extends

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
July 29, 2022· Hobbs Medical, Inc.

Recalled Item: Freeman Pancreatic Flexi-Stent Kits: Single Pigtail (containing 6544)...

The Issue: Device label display an incorrect expiration date, extends

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
July 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Biliary Pigtail Stent Kits (containing 6105) Catalog Number: 6023

The Issue: Device label display an incorrect expiration date, extends

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
July 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Medical Flex-Ez Guide Wire Disposable For endoscopy procedures Ref:

The Issue: Device label display an incorrect expiration date, extends

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
July 29, 2022· Hobbs Medical, Inc.

Recalled Item: Hobbs Medical Polypectomy Snare Catalog Number: 4563

The Issue: Device label display an incorrect expiration date, extends

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing