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 4218142200 of 46,762 recalls

DrugJuly 18, 2013· GlaxoSmithKline, LLC.

Recalled Item: TUMS Recalled by GlaxoSmithKline, LLC. Due to Presence of Foreign...

The Issue: Presence of Foreign Tablets/Capsules: Product labeled TUMS Ultra Assorted...

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

Class III — Low RiskOngoing
Refund
DrugJuly 18, 2013· Vi-Jon, Inc.

Recalled Item: ALCOHOL FREE ANTISEPTIC (cetylpyridinium chloride) Mouth Rinse Recalled by...

The Issue: Microbial Contamination of Non-Sterile Products: This product is being...

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

Class III — Low RiskOngoing
Refund
FoodJuly 18, 2013· Ferrara Candy Company

Recalled Item: Chocolate malted milk balls packaged in 6 lbs. bags and Recalled by Ferrara...

The Issue: One lot of Brach's Chocolate Malted Milk Balls may contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
FoodJuly 18, 2013· Olam Tomato Processors, Inc.

Recalled Item: Medium Chunky Salsa Recalled by Olam Tomato Processors, Inc. Due to The firm...

The Issue: The firm received complaints of large fragments of glass that were found...

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 18, 2013· Olam Tomato Processors, Inc.

Recalled Item: Mild Chunky Salsa Recalled by Olam Tomato Processors, Inc. Due to The firm...

The Issue: The firm received complaints of large fragments of glass that were found...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 18, 2013· Siemens Medical Solutions USA, Inc

Recalled Item: PRIMUS Recalled by Siemens Medical Solutions USA, Inc Due to Siemens has...

The Issue: Siemens has become aware of a customer complaint concerning the rail...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2013· Aspen Surgical Products, Inc.

Recalled Item: Distributed in USA: Product Number: 40-2894: Reinforced Wound Closure...

The Issue: Aspen Surgical is recalling Wound Closures because firm could not confirm...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2013· Vital Signs Devices, a GE Healthcare Company

Recalled Item: Disposable Temperature Probes Recalled by Vital Signs Devices, a GE...

The Issue: GE Healthcare has become aware of a potential safety issue associated with...

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

Class II — Potential Health HazardOngoing
DrugJuly 17, 2013· Apotex Inc.

Recalled Item: Acyclovir Tablets USP 800 mg Recalled by Apotex Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: Product from lot KF2199, may contain tablets...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 17, 2013· Hospira Inc.

Recalled Item: Product is labeled in part: LIST NO. 43449 Recalled by Hospira Inc. Due to...

The Issue: Hospira has recieved reports that the vacuum needed to create suction with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2013· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Custom Perfusion System with Carmeda BioActive Surface. Model...

The Issue: Medtronic was notified that Edwards Lifesciences has initiated a product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2013· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Custom Perfusion System. Model Numbers: 1D80R8 Recalled by...

The Issue: Medtronic was notified that Edwards Lifesciences has initiated a product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2013· Medtronic Inc. Cardiac Rhythm Disease Management

Recalled Item: Medtronic Custom Perfusion System with Trillium BioSurface (a polymer...

The Issue: Medtronic was notified that Edwards Lifesciences has initiated a product...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT and Brilliance iCT SP These systems are intended Recalled by...

The Issue: An artifact that resembles thrombus may appear on the image.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2013· HemoCue AB

Recalled Item: HemoCue¿ Urine Albumin Microcuvettes Recalled by HemoCue AB Due to HemoCue...

The Issue: HemoCue AB has become aware of a production related problem involving...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2013· Aesculap, Inc.

Recalled Item: UNITRAC Pneumatic Retraction Arm. A support arm used to hold Recalled by...

The Issue: Changes were implemented to the UNITRAC instructions for use to ensure safe...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2013· Edwards Lifesciences, LLC

Recalled Item: Edwards EndoReturn Arterial Cannula Recalled by Edwards Lifesciences, LLC...

The Issue: Edwards Lifesciences is recalling certain lots of the EndoReturn Arterial...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2013· Assuramed

Recalled Item: DiaScreen Liquid Urine Controls: Positive and Negative Assayed Liquid...

The Issue: The products may have been stored at temperatures outside their required...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2013· Assuramed

Recalled Item: ProTime Microcoagulation System Recalled by Assuramed Due to The products...

The Issue: The products may have been stored at temperatures outside their required...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2013· Assuramed

Recalled Item: Hemoccult II BRAND SENSA elite Recalled by Assuramed Due to The products may...

The Issue: The products may have been stored at temperatures outside their required...

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

Class II — Potential Health HazardOngoing