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. 2,326 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,326 in last 12 months

Showing 3382133840 of 46,762 recalls

DrugNovember 11, 2015· RemedyRepack Inc.

Recalled Item: Bicillin L-A 600000 Units/mL Inj. Recalled by RemedyRepack Inc. Due to...

The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2015· RemedyRepack Inc.

Recalled Item: Vitamin B-Complex 100 Recalled by RemedyRepack Inc. Due to Labeling:...

The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2015· RemedyRepack Inc.

Recalled Item: Ascorbic Acid 500 MG/ML Inj. Recalled by RemedyRepack Inc. Due to Labeling:...

The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2015· RemedyRepack Inc.

Recalled Item: Novolin 70/30 Recalled by RemedyRepack Inc. Due to Labeling: Incorrect...

The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2015· RemedyRepack Inc.

Recalled Item: Rocuronium Bromide 50 MG/5ML INJ. Recalled by RemedyRepack Inc. Due to...

The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2015· RemedyRepack Inc.

Recalled Item: Lorazepam 2 mg/mL Inj. Recalled by RemedyRepack Inc. Due to Labeling:...

The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 11, 2015· RemedyRepack Inc.

Recalled Item: Humulin 70/30 Recalled by RemedyRepack Inc. Due to Labeling: Incorrect...

The Issue: Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 11, 2015· ConvaTec, Inc

Recalled Item: Nebulizer Masks Opti-Mist and Opti-Mist Clear Nebulizer masks are intended...

The Issue: The Nebulizer mask malfunctions in that there is reduced or no aerosol...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care" CCRP TestPak-in vitro diagnostic product intended to...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care CKMB DilPak- an in vitro diagnostic product Recalled by...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care DDMR TestPak Catalog Number: CDDMRE SMN: 10701511...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care MYO DilPak Catalog Number: CMYO-D SMN:10445081 in...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care" MYO TestPak-in vitro diagnostic test for the Recalled by...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care pBNP TestPak- in vitro diagnostic test for Recalled by...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care CCRP CalPak-in vitro diagnostic product intended to...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care CKMB TestPak- in vitro diagnostic test for Recalled by...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care BHCG CalPak-in vitro diagnostic product intended to...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care BHCG TestPak-an in vitro diagnostic product intended...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 11, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens Acute Care CTNI TestPak-in vitro diagnostic test for the Recalled by...

The Issue: Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems

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

Class II — Potential Health HazardOngoing
DrugNovember 10, 2015· Northwind Pharmaceuticals LLC

Recalled Item: Prednisone 20 mg Recalled by Northwind Pharmaceuticals LLC Due to Labeling:...

The Issue: Labeling: Not elsewhere classified. NDC number is incorrect on the container.

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

Class III — Low RiskOngoing
Refund