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. 2,311 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,311 in last 12 months

Showing 3726137280 of 46,762 recalls

Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Navilyst Medical, Inc

Recalled Item: NAMIC Convenience Kit Recalled by Navilyst Medical, Inc Due to The labelled...

The Issue: The labelled expiration dating of the affected product is not fully...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2015· Arrow International Inc

Recalled Item: Arrow Select Kits (ASK) Recalled by Arrow International Inc Due to Certain...

The Issue: Certain product codes and lot numbers of Kits with Biopatch Dressing were...

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

Class III — Low RiskOngoing
FoodJanuary 9, 2015· The Hain Celestial Group- Worldwide Headquarters

Recalled Item: Taj ETHNIC GOURMET BOMBAY CURRY Simmer Sauce Recalled by The Hain Celestial...

The Issue: Cumin may contain undeclared peanut protein.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 9, 2015· Kellogg USA Inc

Recalled Item: MorningStar Farms Spicy Black Bean Burger: 9.50 oz (4 ct) - Recalled by...

The Issue: Products contain undeclared peanut protein.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 9, 2015· Kellogg USA Inc

Recalled Item: MorningStar Farms Chipotle Black Bean Burger Recalled by Kellogg USA Inc Due...

The Issue: Products contain undeclared peanut protein.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 9, 2015· The Hain Celestial Group- Worldwide Headquarters

Recalled Item: Taj ETHNIC GOURMET CALCUTTA MASALA Simmer Sauce Recalled by The Hain...

The Issue: Cumin may contain undeclared peanut protein.

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 9, 2015· The Hain Celestial Group- Worldwide Headquarters

Recalled Item: Taj ETHNIC GOURMET PUNJAB SAAG Spinach Sauce Recalled by The Hain Celestial...

The Issue: Cumin may contain undeclared peanut protein.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 8, 2015· Freedom Pharmaceuticals Inc

Recalled Item: 5-methyltetrahydrofolate Calcium (L) (a) 1 gm in 2 oz container Recalled by...

The Issue: Subpotent Drug

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 7, 2015· Cincinnati Sub-Zero Products Inc

Recalled Item: Cold Therapy Pad - cold water circulating pad Recalled by Cincinnati...

The Issue: Seals in the water path of the CT-99 cold therapy pad may separate during...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2015· Stryker Instruments Div. of Stryker Corporation

Recalled Item: System 6 Aseptic Housing. The Stryker System 6 Aseptic Housings Recalled by...

The Issue: Stryker is recalling System 6 Aseptic Housing, due to a failed Continuous...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2015· GE Healthcare

Recalled Item: This correction applies to all GE Healthcare MRI systems with Recalled by GE...

The Issue: At certain sites, the MRU may not be connected to the magnet. In emergency...

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

Class I — Serious Health HazardOngoing