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. 2,374 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,374 in last 12 months

Showing 2110121120 of 46,762 recalls

FoodMay 6, 2019· Barlean's Llc

Recalled Item: Item FG 10146 Recalled by Barlean's Llc Due to Undeclared Sulfites

The Issue: Barlean's dietary supplement product is recalled due to undeclared Sulfites....

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

Class III — Low RiskOngoing
Refund
FoodMay 6, 2019· Barlean's Llc

Recalled Item: Item FG 10037 Recalled by Barlean's Llc Due to Undeclared Sulfites

The Issue: Barlean's dietary supplement product is recalled due to undeclared Sulfites....

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

Class III — Low RiskOngoing
Refund
FoodMay 6, 2019· Barlean's Llc

Recalled Item: Item FG 10084 Recalled by Barlean's Llc Due to Undeclared Sulfites

The Issue: Barlean's dietary supplement product is recalled due to undeclared Sulfites....

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

Class III — Low RiskOngoing
Refund
FoodMay 6, 2019· Barlean's Llc

Recalled Item: Item FG 10083 Recalled by Barlean's Llc Due to Undeclared Sulfites

The Issue: Barlean's dietary supplement product is recalled due to undeclared Sulfites....

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

Class III — Low RiskOngoing
Refund
FoodMay 6, 2019· Barlean's Llc

Recalled Item: Item FG 10149 Recalled by Barlean's Llc Due to Undeclared Sulfites

The Issue: Barlean's dietary supplement product is recalled due to undeclared Sulfites....

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

Class III — Low RiskOngoing
Refund
FoodMay 6, 2019· Barlean's Llc

Recalled Item: Item FG 10085 Recalled by Barlean's Llc Due to Undeclared Sulfites

The Issue: Barlean's dietary supplement product is recalled due to undeclared Sulfites....

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

Class III — Low RiskOngoing
Refund
FoodMay 6, 2019· Barlean's Llc

Recalled Item: Item FG 10106 Recalled by Barlean's Llc Due to Undeclared Sulfites

The Issue: Barlean's dietary supplement product is recalled due to undeclared Sulfites....

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

Class III — Low RiskOngoing
Refund
FoodMay 6, 2019· Barlean's Llc

Recalled Item: Item FG 10190 Recalled by Barlean's Llc Due to Undeclared Sulfites

The Issue: Barlean's dietary supplement product is recalled due to undeclared Sulfites....

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

Class III — Low RiskOngoing
Refund
FoodMay 6, 2019· Barlean's Llc

Recalled Item: Item FG 10089 Recalled by Barlean's Llc Due to Undeclared Sulfites

The Issue: Barlean's dietary supplement product is recalled due to undeclared Sulfites....

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

Class III — Low RiskOngoing
Refund
FoodMay 6, 2019· Barlean's Llc

Recalled Item: Item FG 10191 Recalled by Barlean's Llc Due to Undeclared Sulfites

The Issue: Barlean's dietary supplement product is recalled due to undeclared Sulfites....

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

Class III — Low RiskOngoing
Refund
FoodMay 6, 2019· Barlean's Llc

Recalled Item: Item FG 10116 Recalled by Barlean's Llc Due to Undeclared Sulfites

The Issue: Barlean's dietary supplement product is recalled due to undeclared Sulfites....

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 6, 2019· Becton Dickinson & Company

Recalled Item: Alaris Pump Infusion Set Recalled by Becton Dickinson & Company Due to An...

The Issue: An incomplete occlusion can be caused by a variation in the wall thickness...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 6, 2019· Qiagen Sciences, Inc.

Recalled Item: RNeasy DSP FFPE Kit (48) Recalled by Qiagen Sciences, Inc. Due to The...

The Issue: The deparaffinization solution contains a contaminant, which leads to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2019· Maquet Cardiovascular Us Sales, Llc

Recalled Item: GETINGE MEERA MOBILE OPERATING TABLE: (1) Part 720001B2 (2) Part Recalled by...

The Issue: User may suffer an electric shock when coming in contact with the exposed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2019· NeuroLogica Corporation

Recalled Item: Samsung GM85 Mobile Digital X-ray Imaging System Product Usage: The Recalled...

The Issue: Potential issue related to the operation of the safety latch within the...

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

Class II — Potential Health HazardOngoing
DrugMay 3, 2019· Avella of Deer Valley, Inc. Store 38

Recalled Item: Bevacizumab 2.5 mg/0.1 mL Recalled by Avella of Deer Valley, Inc. Store 38...

The Issue: Lack of assurance of sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 3, 2019· Heritage Pharmaceuticals, Inc.

Recalled Item: Losartan Potassium Tablets USP 100 mg 90 film coated tablets Recalled by...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 3, 2019· Heritage Pharmaceuticals, Inc.

Recalled Item: Losartan Potassium Tablets USP 50 mg 90 film coated tablets Recalled by...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 3, 2019· Heritage Pharmaceuticals, Inc.

Recalled Item: Losartan Potassium Tablets USP 25 mg 90 film coated tablets Recalled by...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 3, 2019· Heritage Pharmaceuticals, Inc.

Recalled Item: Losartan Potassium Tablets USP 100 mg 1000 film coated tablets Recalled by...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund