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. 2,251 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,251 in last 12 months

Showing 4440144420 of 46,762 recalls

Medical DeviceDecember 5, 2012· SynCardia Systems Inc.

Recalled Item: Companion External Battery Recalled by SynCardia Systems Inc. Due to...

The Issue: Syncardia Systems is recalling the Companion External Batteries used with...

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

Class II — Potential Health HazardOngoing
DrugDecember 4, 2012· Green Valley Drugs

Recalled Item: Cyanocobalamin 1000 mcg/ml Recalled by Green Valley Drugs Due to...

The Issue: Non-Sterility: Green Valley Drugs received positive sterility results from...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 4, 2012· Green Valley Drugs

Recalled Item: Methylprednisolone Preservative Free 40 mg/ml Injectible Suspension Recalled...

The Issue: Non-Sterility: Green Valley Drugs received positive sterility results from...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 4, 2012· Amedra Pharmaceuticals LLC

Recalled Item: Dextroamphetamine Sulfate Extended Release Capsules Recalled by Amedra...

The Issue: Failed Dissolution Specifications: The affected lots may not meet the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 4, 2012· Amedra Pharmaceuticals LLC

Recalled Item: Dextroamphetamine Sulfate Extended Release Capsules Recalled by Amedra...

The Issue: Failed Dissolution Specifications: The affected lots may not meet the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 4, 2012· Amedra Pharmaceuticals LLC

Recalled Item: Dextroamphetamine Sulfate Extended Release Capsules Recalled by Amedra...

The Issue: Failed Dissolution Specifications: The affected lots may not meet the...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 4, 2012· Abbott Laboratories

Recalled Item: Synthroid (Levothyroxine Sodium) tablets Recalled by Abbott Laboratories Due...

The Issue: Labeling: Error on Declared Strength. Product labeled to contain 150 mcg...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 4, 2012· Johnson & Johnson

Recalled Item: Clean & Clear advantage Recalled by Johnson & Johnson Due to Superpotent...

The Issue: Superpotent (Single Ingredient Drug): salicylic acid

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 4, 2012· Abbott Molecular

Recalled Item: Abbott m2000sp Instrument Recalled by Abbott Molecular Due to An issue with...

The Issue: An issue with the m2000sp Instrument software has been identified whereby,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· Quidel Corporation

Recalled Item: Quidel Recalled by Quidel Corporation Due to Quidel Corporation has...

The Issue: Quidel Corporation has initiated a voluntary recall of specific lots of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· DePuy Orthopaedics, Inc.

Recalled Item: SOL SYS 8IN CALC 1.5/18.0 Packaging: Product is packed within Recalled by...

The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· DePuy Orthopaedics, Inc.

Recalled Item: SOL SYS L 9IN CALC 2.25/15.0 Packaging: Product is packed Recalled by DePuy...

The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· DePuy Orthopaedics, Inc.

Recalled Item: SOL SYS R 9IN CALC 2.25/16.5 Packaging: Product is packed Recalled by DePuy...

The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· DePuy Orthopaedics, Inc.

Recalled Item: SOL SYS 8IN CALC 1.5/19.5 Packaging: Product is packed within Recalled by...

The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· DePuy Orthopaedics, Inc.

Recalled Item: SOL SYS L 9IN CALC 2.25/19.5 Packaging: Product is packed Recalled by DePuy...

The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· Medtronic Neuromodulation

Recalled Item: Medtronic Recalled by Medtronic Neuromodulation Due to Medtronic has...

The Issue: Medtronic has identified 140 Restore DBS Extension Kits (model numbers 7482,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· DePuy Orthopaedics, Inc.

Recalled Item: SOL SYS F 8 CALC 13.5MM LG Packaging: Product is Recalled by DePuy...

The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· DePuy Orthopaedics, Inc.

Recalled Item: SOL SYS R 9IN CALC 2.25/18 Packaging: Product is packed Recalled by DePuy...

The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· DePuy Orthopaedics, Inc.

Recalled Item: SOL SYS R 9IN CALC 2.25/21 Packaging: Product is packed Recalled by DePuy...

The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2012· DePuy Orthopaedics, Inc.

Recalled Item: SOL SYS R 9IN CALC 2.25/19.5 Packaging: Product is packed Recalled by DePuy...

The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...

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

Class II — Potential Health HazardOngoing