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. 2,283 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,283 in last 12 months

Showing 541560 of 46,762 recalls

Medical DeviceDecember 4, 2025· Merit Medical Systems, Inc.

Recalled Item: Merit Medical Recalled by Merit Medical Systems, Inc. Due to Inflation...

The Issue: Inflation device handle may detach from the syringe during procedure.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2025· Merit Medical Systems, Inc.

Recalled Item: Merit Medical Recalled by Merit Medical Systems, Inc. Due to Inflation...

The Issue: Inflation device handle may detach from the syringe during procedure.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2025· Merit Medical Systems, Inc.

Recalled Item: Allwell Inflation Device Recalled by Merit Medical Systems, Inc. Due to...

The Issue: Inflation device handle may detach from the syringe during procedure.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2025· Mobius Imaging, LLC

Recalled Item: Detachable 10in Pend FRU-1 Pend component for the AIRO Computed Recalled by...

The Issue: AIRO pendant replacement kits and upgrade do not possess the "Safe Hand...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2025· Medtronic Inc

Recalled Item: Abre Venous Self-Expanding Stent System Recalled by Medtronic Inc Due to...

The Issue: Stents may be impacted by a Nitinol anomaly which causes a reduced stent...

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

Class II — Potential Health HazardOngoing
FoodDecember 4, 2025· AZ Gems, Inc.

Recalled Item: Jumbo RAW SHRIMP Recalled by AZ Gems, Inc. Due to elevated levels of...

The Issue: elevated levels of chloramphenicol in frozen shrimp

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Ingenia 1.5T. Product Code (REF): (1) 781341 Recalled by Philips North...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Upgrade to MR 7700. Product Code (REF): 782130. MR systems Recalled by...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· CareFusion 303, Inc.

Recalled Item: BD Pyxis ES Enterprise Server Catalog Numbers 1115-00 Recalled by CareFusion...

The Issue: Due a software issue that may result in equipment not receiving timely...

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

Class II — Potential Health HazardOngoing
FoodDecember 3, 2025· McCain Foods USA Inc

Recalled Item: Ore-Ida Tater Tots shaped potatoes Recalled by McCain Foods USA Inc Due to...

The Issue: Clear hard plastic fragments.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 3, 2025· Medtronic Neuromodulation

Recalled Item: A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465 and...

The Issue: Complaints received that Vanta A71200 CP App does not function as intended...

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

Class II — Potential Health HazardOngoing
FoodDecember 3, 2025· McCain Foods USA Inc

Recalled Item: Sysco Imperial Potato Tater Barrel Recalled by McCain Foods USA Inc Due to...

The Issue: Clear hard plastic fragments.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 3, 2025· Boston Scientific Corporation

Recalled Item: Boston Scientific Coyote OVER-THE-WIRE PTA Balloon Dilation Catheter...

The Issue: Boston Scientific is initiating the removal of certain batches of Coyote"...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Ingenia Elition S. Product Code (REF): (1) 781357 Recalled by Philips North...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Ingenia Ambition X. Product Code (REF): (1) 781356 Recalled by Philips North...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: SmartPath to dStream for XR and 3.0T. Product Code (REF): Recalled by...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Evolution Upgrade 3.0T. Product Code (REF): 782143. MR systems with Recalled...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Ingenia Elition X. Product Code (REF): (1) 781358 Recalled by Philips North...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: Ingenia 3.0T CX. Product Code (REF): 781271. MR systems with Recalled by...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2025· Philips North America

Recalled Item: MR 7700. Product Code (REF): (1) 782120 Recalled by Philips North America...

The Issue: The potential for stiffness value errors when viewing exported MR...

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

Class II — Potential Health HazardOngoing