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. 2,550 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,550 in last 12 months

Showing 13611380 of 46,762 recalls

DrugSeptember 4, 2025· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Entecavir Tablets Recalled by Zydus Pharmaceuticals (USA) Inc Due to Failed...

The Issue: Failed Impurity/Degradation Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits Item Number/Description HSAN63N ANGIO PACK IHAN02W...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits Item Number/Description BFCT04X CATARACT PACK -...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits Item Number/Description BUCY78E CYSTO PACK CMCP10X...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits Item number/ Product description AHLD15X LABOR...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits IHDC30R D AND C PACK Recalled by American Contract...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Basic Biopsy Tray Recalled by American Contract Systems Inc. Due to...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits Item Number/Description ANSH14AF SHOULDER PACK -...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Basic Biopsy Tray Recalled by American Contract Systems Inc. Due to...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits UDPG88W PICC G-TUBE PACK-230209 Recalled by...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits Item Number/Description LKRA40G RADIOLOGY PACK...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits Item Number/Description EVLH67F LEFT HEART CATH...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits Item Number/Description FHCP08Y C SECTION PK...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· Lutronic Corporation

Recalled Item: XERF EFFECTOR 60. Electrosurgical unit. Recalled by Lutronic Corporation Due...

The Issue: Manufacturing defects in devices manufactured from 4/1/25 to 8/20/25 can on...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits Item number/ Product description AKGN82E GENERAL...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits Item Number/Description ANCV78BC HEART PACK -...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· Contego Medical LLC

Recalled Item: Neuroguard IEP 3 in 1 Carotid Stent and Post-Dilation Balloon Recalled by...

The Issue: Carotid stent and post-dilation balloon system with integrated embolic...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits Item Number/Description HSLM53AB SPINE PACK MILM82A...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits Item Number/Description RCEN25B ENT SDSC 0246972...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 4, 2025· American Contract Systems Inc.

Recalled Item: Medical convenience kits Item Number/Description UICL44P ADULT CENTRAL LINE...

The Issue: Identified products were re-gassed (sterilized more than once) after a...

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

Class II — Potential Health HazardOngoing