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 4238142400 of 46,762 recalls

DrugJune 18, 2013· Novartis Consumer Health

Recalled Item: Theraflu Flu & Sore Throat (acetaminophen 650 mg Recalled by Novartis...

The Issue: Presence of Foreign Substance: The products are being recalled because they...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Methylphenidate Hydrochloride Extended-Release Capsules (LA) Recalled by...

The Issue: Failed Dissolution Specifications: Product is being recalled due to out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Methylphenidate Hydrochloride Extended-Release Capsules (LA) Recalled by...

The Issue: Failed Dissolution Specifications: Product is being recalled due to out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Methylphenidate Hydrochloride Extended-Release Capsules (LA) Recalled by...

The Issue: Failed Dissolution Specifications: Product is being recalled due to out of...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 18, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Amoxicillin for Oral Suspension Recalled by Teva Pharmaceuticals USA, Inc....

The Issue: Discoloration: This recall is being carried out due to an orange to brown...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJune 18, 2013· Invacare Corporation

Recalled Item: CHAMPION Medical Recliner Recalled by Invacare Corporation Due to There is a...

The Issue: There is a possibility of elevated temperatures in the seat pad. In...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 18, 2013· Hospira Inc.

Recalled Item: LifeShield Recalled by Hospira Inc. Due to Hospira has received reports of...

The Issue: Hospira has received reports of customers experiencing air-in-line alarms...

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

Class II — Potential Health HazardOngoing
DrugJune 17, 2013· Advance Pharmaceutical Inc

Recalled Item: ENTERIC COATED ASPIRIN (NSAID) Recalled by Advance Pharmaceutical Inc Due to...

The Issue: Labeling: Label Mix-Up: A complaint from a pharmacist was received that the...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 17, 2013· Nanosphere, Inc.

Recalled Item: Verigene BC-GN Kit (Catalog number 20-005-021) Recalled by Nanosphere, Inc....

The Issue: There is a specific Extraction Tray lot containing Tips that may slightly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2013· Nanosphere, Inc.

Recalled Item: Verigene BC-GP Kit (Catalog number 20-005-018) Recalled by Nanosphere, Inc....

The Issue: There is a specific Extraction Tray lot containing Tips that may slightly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2013· CareFusion 303, Inc.

Recalled Item: Alaris PC unit Recalled by CareFusion 303, Inc. Due to CareFusion is...

The Issue: CareFusion is recalling the Alaris PC units model 8015 (PC unit), version...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 16, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: The SurgiCounter Charging Cradle Product Usage: SurgiCounter Charging...

The Issue: Faulty SurgiCounter Charging Cradle can prevent the scanner from charging or...

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

Class II — Potential Health HazardOngoing
DrugJune 14, 2013· Boehringer Ingelheim Roxane Inc

Recalled Item: Prednisone Tablet USP Recalled by Boehringer Ingelheim Roxane Inc Due to...

The Issue: Labeling: Missing Label; missing label on blister card

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

Class III — Low RiskOngoing
Refund
FoodJune 14, 2013· See's Candies Inc.

Recalled Item: See's Dark Raisins: Ingredients: Raisins Recalled by See's Candies Inc. Due...

The Issue: Potential for nuts and/or nut and egg residue may be present in some of the...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 14, 2013· See's Candies Inc.

Recalled Item: See's Milk Raisins: Ingredients: Raisins Recalled by See's Candies Inc. Due...

The Issue: Potential for nuts and/or nut and egg residue may be present in some of the...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 14, 2013· PIONEER SURGICAL TECHNOLOGY, INC.

Recalled Item: Streamline MIS Spinal Fixation System Fixed Rod Holder NON STERILE Recalled...

The Issue: The affected fixed rod holders did not allow the instrument to lock down on...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 14, 2013· Biomerieux Inc

Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...

The Issue: A product issue has been identified for customers using software version...

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

Class II — Potential Health HazardOngoing