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 4418144200 of 46,762 recalls

FoodJanuary 19, 2013· Pamela's Products, Inc.

Recalled Item: Pamela's Baking and Pancake Mix Recalled by Pamela's Products, Inc. Due to...

The Issue: Firm received complaints for on four (4) products which may contain glass or...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 19, 2013· Pamela's Products, Inc.

Recalled Item: Pamela's Chocolate Chunk Cookie Mix Recalled by Pamela's Products, Inc. Due...

The Issue: Firm received complaints for on four (4) products which may contain glass or...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 18, 2013· NBTY Inc.

Recalled Item: MET-Rx EXTREME NOS PUMPED DOUBLE BERRY Naturally and Artificially Flavored...

The Issue: The color, odor, and taste of the products are changing and do not meet the...

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

Class III — Low RiskOngoing
Refund
FoodJanuary 18, 2013· NBTY Inc.

Recalled Item: MET-Rx EXTREME NOS PUMPED NITRO-PUNCH Naturally Flavored DIETARY SUPPLEMENT...

The Issue: The color, odor, and taste of the products are changing and do not meet the...

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

Class III — Low RiskOngoing
Refund
FoodJanuary 18, 2013· NBTY Inc.

Recalled Item: MET-Rx EXTREME NOS PUMPED WATERMELON Naturally and Artificially Flavored...

The Issue: The color, odor, and taste of the products are changing and do not meet the...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 18, 2013· Aesculap, Inc.

Recalled Item: Aesculap Bipolar Generator Foot Pedal Recalled by Aesculap, Inc. Due to The...

The Issue: The bipolar energy did not stop after release of the foot pedal.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2013· Elekta, Inc.

Recalled Item: Elekta Recalled by Elekta, Inc. Due to If the Apex collimator is incorrectly...

The Issue: If the Apex collimator is incorrectly installed on the radiation head, a...

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

Class II — Potential Health HazardOngoing
DrugJanuary 18, 2013· Aaron Industries Inc

Recalled Item: Rite Aid Maximum Strength Tussin Cough & Cold Mucus Relief CF Recalled by...

The Issue: Presence of Precipitate; white substance confirmed as Guaifenesin, an active...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 18, 2013· Aaron Industries Inc

Recalled Item: Well at Walgreens Wal-Tussin CF Max Recalled by Aaron Industries Inc Due to...

The Issue: Presence of Precipitate; white substance confirmed as Guaifenesin, an active...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 18, 2013· Aaron Industries Inc

Recalled Item: Wal-Mart Equate Tussin CF Adult Maximum Strength Recalled by Aaron...

The Issue: Presence of Precipitate; white substance confirmed as Guaifenesin, an active...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 18, 2013· Aaron Industries Inc

Recalled Item: Select Brand Cough Control CF Max Recalled by Aaron Industries Inc Due to...

The Issue: Presence of Precipitate; white substance confirmed as Guaifenesin, an active...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 18, 2013· CHENICA INC.

Recalled Item: Chenica Gunnell Rehab Series of Wheelchairs (GRSW) Recalled by CHENICA INC....

The Issue: The wheelchairs may not meet the specifications of WC-19 (crash testing),...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2013· St Jude Medical Inc

Recalled Item: St. Jude Medical Recalled by St Jude Medical Inc Due to The distal end of...

The Issue: The distal end of the core wire of the TorqVue FX Delivery System could...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 17, 2013· Carestream Health, Inc.

Recalled Item: KODAK INSIGHT DENTAL FILM in SureSoft Packets Recalled by Carestream Health,...

The Issue: Missing symbols and manufacturing information on the clear carton label. The...

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

Class III — Low RiskOngoing
DrugJanuary 17, 2013· Humco Holding Group, Inc

Recalled Item: Mercuroclear Antiseptic Anesthetic First Aid Helps prevent infection and...

The Issue: Microbial Contamination of Non-Sterile Product(s): The product has the...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 17, 2013· Walong Marketing, Inc.

Recalled Item: Tausi Brand Salted Black Beans Recalled by Walong Marketing, Inc. Due to...

The Issue: Walong is recalling Tausi Brand Salted Black Beans because it may have the...

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

Class III — Low RiskOngoing
Refund
Medical DeviceJanuary 17, 2013· Ormco/Sybronendo

Recalled Item: SybronEndo Elements Obturation Unit Recalled by Ormco/Sybronendo Due to A...

The Issue: A recall has been issued by SybronEndo because a Canadian Standards...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2013· Ormco/Sybronendo

Recalled Item: SybronEndo Replacement AC Power Cord Recalled by Ormco/Sybronendo Due to A...

The Issue: A recall has been issued by SybronEndo because a Canadian Standards...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2013· Philips Healthcare Inc.

Recalled Item: Philips BuckyDiagnost Radiographic. Catalog Numbers: 704031 Recalled by...

The Issue: An inspection of IATD (Installation Acceptance Test Document)IA SID (Source...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2013· Philips Healthcare Inc.

Recalled Item: Philips Diagnost Stationary Radiographic System Models: 712020 Recalled by...

The Issue: Installation Acceptance Test Document (IATD) non compliant with regulations....

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

Class II — Potential Health HazardOngoing