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. 1,882 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
1,882 in last 12 months

Showing 71417160 of 46,762 recalls

Medical DeviceNovember 7, 2023· GE Hangwei Medical Systems, Co. LTD

Recalled Item: The System is designed as a modular system with components Recalled by GE...

The Issue: GE HealthCare has become aware of the potential that incorrect torque has...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Abiomed, Inc.

Recalled Item: Abiomed KIT Recalled by Abiomed, Inc. Due to Hole(s) to the outer pouch of...

The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Abiomed, Inc.

Recalled Item: Abiomed Introducer Kit Recalled by Abiomed, Inc. Due to Hole(s) to the outer...

The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Abiomed, Inc.

Recalled Item: Abiomed Kit Recalled by Abiomed, Inc. Due to Hole(s) to the outer pouch of...

The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Abiomed, Inc.

Recalled Item: Oscor Intro Kit Recalled by Abiomed, Inc. Due to Hole(s) to the outer pouch...

The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Luminex Corporation

Recalled Item: Luminex VERIGENE BC-GP Utility Tray (5-Pack Carrier) Recalled by Luminex...

The Issue: Potentially defective utility trays in the reagent kits.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Abiomed, Inc.

Recalled Item: Abiomed Kit Recalled by Abiomed, Inc. Due to Hole(s) to the outer pouch of...

The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Abiomed, Inc.

Recalled Item: Abiomed Axillary Insertion Introducer -Introducer(s) are intended for...

The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2023· Abiomed, Inc.

Recalled Item: Abiomed Kit Recalled by Abiomed, Inc. Due to Hole(s) to the outer pouch of...

The Issue: Hole(s) to the outer pouch of the Introducer Kits (both trayed and...

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

Class II — Potential Health HazardOngoing
DrugNovember 7, 2023· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Indomethacin 25mg Capsules Recalled by Glenmark Pharmaceuticals Inc., USA...

The Issue: Labeling: Label Mix-Up-Indomethacin bottles may be labeled as Naproxen

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 7, 2023· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Naproxen Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: Labeling: Label Mix-Up-Indomethacin bottles may be labeled as Naproxen

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 6, 2023· Taro Pharmaceuticals Inc.

Recalled Item: Hydrocortisone 1% and Acetic Acid 2% Otic Solution USP Recalled by Taro...

The Issue: Failed Impurities/Degradation Specifications:Out-of-Specification result for...

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

Class III — Low RiskOngoing
Refund
DrugNovember 6, 2023· Bayer Healthcare Pharmaceuticals Inc.

Recalled Item: VITRAKVI (larotractenib) oral solution Recalled by Bayer Healthcare...

The Issue: Microbial Contamination of Non-Sterile Products: microbial contamination...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 6, 2023· Nurse Assist, LLC

Recalled Item: Sterile Water/Saline: Product Name/Product Code: CUP STERILE WATER¿ FOIL LID...

The Issue: Sodium chloride irrigation USP, and sterile water for irrigation USP, that...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 6, 2023· Physio-Control, Inc.

Recalled Item: AC Power Adapter for use with the LIFEPAK 15 Monitor/Defibrillator Recalled...

The Issue: AC Power Adapter (ACPA) may not charge the monitor/defibrillator batteries...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2023· Nurse Assist, LLC

Recalled Item: Sterile Water/Saline: Brand Name: Product Name/Product Code: CARDINAL: 100ML...

The Issue: Sodium chloride irrigation USP, and sterile water for irrigation USP, that...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 6, 2023· Nurse Assist, LLC

Recalled Item: 0.9% Sodium Chloride: Product Name/Product Code: 10ML IV FLUSH STERILE...

The Issue: Sodium chloride irrigation USP, and sterile water for irrigation USP, that...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 6, 2023· Nurse Assist, LLC

Recalled Item: Sterile Water: Product Name/Product Code: USP STERILE WATER SYRINGE/1030A...

The Issue: Sodium chloride irrigation USP, and sterile water for irrigation USP, that...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 6, 2023· Maquet Medical Systems USA

Recalled Item: CARDIOHELP-i Heart Lung Support System- A blood oxygenation and carbon...

The Issue: Certain factory settings for the device were incorrectly described in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 6, 2023· Merit Medical Systems, Inc.

Recalled Item: Fountain Recalled by Merit Medical Systems, Inc. Due to The sterility of...

The Issue: The sterility of microcatheter and infusion system devices cannot be guaranteed.

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

Class II — Potential Health HazardOngoing