Product Recalls in Alaska

Product recalls affecting Alaska — including food, drugs, consumer products, medical devices, and vehicles distributed to Alaska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,506 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,506 in last 12 months

Showing 1092110940 of 46,762 recalls

Medical DeviceJuly 29, 2022· Hobbs Medical, Inc.

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

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

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

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

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 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 the shelf life of...

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

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

Recalled Item: Freeman Pancreatic Flexi-Stent Catalog Number: 6535 Recalled by Hobbs...

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

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

Recalled Item: Hobbs Scope Introducer Catalog Number: 4650 Recalled by Hobbs Medical, Inc....

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

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

Recalled Item: Hobbs Medical Polypectomy Snare Catalog Number: 7202 Recalled by Hobbs...

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 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 the shelf life of...

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

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

Recalled Item: Hobbs Helical Retrieval Basket Catalog Number: 4814 Recalled by Hobbs...

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

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

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

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

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

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

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 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 the shelf life of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 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 the shelf life of...

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

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

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

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

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

Recalled Item: Hobbs Medical Polypectomy Snare Catalog Number: 4563 Recalled by Hobbs...

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

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

Recalled Item: Hobbs Posi-Stop Injection Needle Catalog Number: 4712 Recalled by Hobbs...

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

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

Recalled Item: Freeman Pancreatic Flexi-Stent Catalog Number: 6566 Recalled by Hobbs...

The Issue: Device label display an incorrect expiration date, extends the shelf life of...

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

Class II — Potential Health HazardOngoing
DrugJuly 28, 2022· Lupin Pharmaceuticals Inc.

Recalled Item: Rifampin Capsules Recalled by Lupin Pharmaceuticals Inc. Due to CGMP...

The Issue: CGMP Deviations:OOS result was observed in 1-Methyl-4-Nitroso Piperazine...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2022· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Divalproex Sodium Extended Release Tablets Recalled by Amneal...

The Issue: Failed dissolution specifications.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJuly 27, 2022· Amerisource Health Services LLC

Recalled Item: Azacitidine for Injection Recalled by Amerisource Health Services LLC Due to...

The Issue: Subpotent Drug

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceJuly 27, 2022· Diasol, Inc

Recalled Item: Diasol Acid Concentrate 100 Recalled by Diasol, Inc Due to Due to labeling...

The Issue: Due to labeling issue. The box label is different that the gallon label in...

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

Class II — Potential Health HazardOngoing