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. 1,648 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
1,648 in last 12 months

Showing 4234142360 of 46,762 recalls

DrugJune 21, 2013· Tween Brands Inc

Recalled Item: Shine from within blueberry Anti bac Justice Recalled by Tween Brands Inc...

The Issue: Labeling: Label Error on Declared Strength; the label states that the...

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

Class III — Low RiskOngoing
Refund
DrugJune 21, 2013· Tween Brands Inc

Recalled Item: I love to shop Justice Recalled by Tween Brands Inc Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength; the label states that the...

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

Class III — Low RiskOngoing
Refund
DrugJune 21, 2013· Tween Brands Inc

Recalled Item: YOU CANT HANDLE THIS Justice Recalled by Tween Brands Inc Due to Labeling:...

The Issue: Labeling: Label Error on Declared Strength; the label states that the...

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

Class III — Low RiskOngoing
Refund
DrugJune 21, 2013· Tween Brands Inc

Recalled Item: I love my BFF Justice Recalled by Tween Brands Inc Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength; the label states that the...

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

Class III — Low RiskOngoing
Refund
DrugJune 21, 2013· Tween Brands Inc

Recalled Item: Share a Smile Mixed berry Anti bac Justice Recalled by Tween Brands Inc Due...

The Issue: Labeling: Label Error on Declared Strength; the label states that the...

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

Class III — Low RiskOngoing
Refund
DrugJune 21, 2013· Tween Brands Inc

Recalled Item: BFF's are COOL! Justice Recalled by Tween Brands Inc Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength; the label states that the...

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

Class III — Low RiskOngoing
Refund
DrugJune 21, 2013· Tween Brands Inc

Recalled Item: I love sleep overs Justice Recalled by Tween Brands Inc Due to Labeling:...

The Issue: Labeling: Label Error on Declared Strength; the label states that the...

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

Class III — Low RiskOngoing
Refund
DrugJune 21, 2013· Tween Brands Inc

Recalled Item: I MUSTACHE YOU TO BE MY BFF Justice Recalled by Tween Brands Inc Due to...

The Issue: Labeling: Label Error on Declared Strength; the label states that the...

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

Class III — Low RiskOngoing
Refund
DrugJune 21, 2013· Bracco Diagnostics Inc

Recalled Item: Gastrografin (Diatrizoate Meglumine and Diatrizoate Sodium Solution)...

The Issue: Presence of foreign substance: One lot of the product may contain black...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 20, 2013· Haemonetics Corporation

Recalled Item: TEG 5000 Thromboelastograph Coagulation Analyzer Product Usage: Multipurpose...

The Issue: Research Use Only (RUO) parameters were included in TEG 5000 User Manual.

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

Class II — Potential Health HazardOngoing
FoodJune 20, 2013· Beta Labs

Recalled Item: Oxyphen XR Recalled by Beta Labs Due to The products contain DMAA, also...

The Issue: The products contain DMAA, also known as 1,3-dimethylamylamine,...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 20, 2013· Beta Labs

Recalled Item: PHEnFX (TM) Recalled by Beta Labs Due to The products contain DMAA, also...

The Issue: The products contain DMAA, also known as 1,3-dimethylamylamine,...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 20, 2013· Beta Labs

Recalled Item: PHENTALENE (TM) Recalled by Beta Labs Due to The products contain DMAA, also...

The Issue: The products contain DMAA, also known as 1,3-dimethylamylamine,...

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 20, 2013· Beta Labs

Recalled Item: RED VIPERS Recalled by Beta Labs Due to The products contain DMAA, also...

The Issue: The products contain DMAA, also known as 1,3-dimethylamylamine,...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 19, 2013· Astellas Pharma US Inc

Recalled Item: AmBisome (amphotericin B) liposome for injection Recalled by Astellas Pharma...

The Issue: Lack of Assurance of Sterility; Astellas Pharma US, Inc. is performing a...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 19, 2013· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista 500 and Dimension Vista 1500 System Aliquot Well Recalled by...

The Issue: Siemens is conducting a field correction for Dimension Vista 500 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2013· Zimmer, Inc.

Recalled Item: VERSA-FX II FEMORAL FIXATION SYSTEM COMPRESSION TUBE/PLATE Recalled by...

The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2013· Zimmer, Inc.

Recalled Item: Free Lock Femoral Hip Fixation System Compression Tube/Plate Recalled by...

The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2013· Zimmer, Inc.

Recalled Item: VERSA-FX II FEMORAL FIXATION SYSTEM COMPRESSION TUBE/PLATE Recalled by...

The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 19, 2013· Zimmer, Inc.

Recalled Item: VERSA-FX FEMORAL FIXATION SYSTEM COMPRESSION LAG SCREW Recalled by Zimmer,...

The Issue: Single packaging configuration used for the VERSA-FX-II Femoral Fixation...

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

Class II — Potential Health HazardOngoing