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. 2,430 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,430 in last 12 months

Showing 1894118960 of 46,762 recalls

Medical DeviceNovember 21, 2019· DeRoyal Industries Inc

Recalled Item: DeRoyal KNEE BRACE Recalled by DeRoyal Industries Inc Due to The Warrior...

The Issue: The Warrior Recovery Knee Brace has the potential to come apart due to the...

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

Class II — Potential Health HazardOngoing
DrugNovember 20, 2019· American Health Packaging

Recalled Item: Ranitidine Tablets Recalled by American Health Packaging Due to CGMP...

The Issue: CGMP Deviations: Potential N-Nitrosodimethylamine (NDMA) amounts above...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 20, 2019· Idelle Labs

Recalled Item: SURE 48 hr Confidence Unscented invisible solid Anti-Perspirant & Deodorant...

The Issue: Labeling Product Contains Undeclared API: Active Ingredient on label is not...

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

Class III — Low RiskOngoing
Refund
DrugNovember 20, 2019· Idelle Labs

Recalled Item: SURE 48hr Confidence Regular Original Solid Anti-Perspirant & Deodorant Net...

The Issue: Labeling Product Contains Undeclared API: Active Ingredient on label is not...

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

Class III — Low RiskOngoing
Refund
DrugNovember 20, 2019· Idelle Labs

Recalled Item: SURE 48hr Confidence Nourishing Coconut invisible solid Antiperspirant &...

The Issue: Labeling Product Contains Undeclared API: Active Ingredient on label is not...

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

Class III — Low RiskOngoing
Refund
DrugNovember 20, 2019· Idelle Labs

Recalled Item: SURE 48hr Confidence Unscented Original Solid Anti-Perspirant & Deodorant...

The Issue: Labeling Product Contains Undeclared API: Active Ingredient on label is not...

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

Class III — Low RiskOngoing
Refund
DrugNovember 20, 2019· AuroMedics Pharma LLC

Recalled Item: Mirtazapine Tablets Recalled by AuroMedics Pharma LLC Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength; cases labelled Mirtazapine 15mg...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 20, 2019· AuroMedics Pharma LLC

Recalled Item: Mirtazapine Tablets Recalled by AuroMedics Pharma LLC Due to Labeling: Label...

The Issue: Labeling: Label Error on Declared Strength; cases labelled Mirtazapine 15mg...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 20, 2019· B. Braun Medical, Inc.

Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...

The Issue: Potential for leakage at the joint between the blood filters and tubing

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2019· B. Braun Medical, Inc.

Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...

The Issue: Potential for leakage at the joint between the blood filters and tubing

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2019· B. Braun Medical, Inc.

Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...

The Issue: Potential for leakage at the joint between the blood filters and tubing

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2019· B. Braun Medical, Inc.

Recalled Item: Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to Potential for...

The Issue: Potential for leakage at the joint between the blood filters and tubing

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2019· Datascope Corporation

Recalled Item: Reinforced Introducer Sets Maquet 8 Fr. Recalled by Datascope Corporation...

The Issue: Potential for compromised sterility in breached pouches of specific lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2019· B. Braun Medical, Inc.

Recalled Item: Safeline Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to...

The Issue: Potential for leakage at the joint between the blood filters and tubing

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2019· B. Braun Medical, Inc.

Recalled Item: Safeline Y-Type Blood Set Recalled by B. Braun Medical, Inc. Due to...

The Issue: Potential for leakage at the joint between the blood filters and tubing

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2019· B. Braun Medical, Inc.

Recalled Item: Outlook Safety Infusion System Y-type Blood Set Recalled by B. Braun...

The Issue: Potential for leakage at the joint between the blood filters and tubing

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2019· Datascope Corporation

Recalled Item: Reinforced Introducer Sets Maquet 7 Fr. Recalled by Datascope Corporation...

The Issue: Potential for compromised sterility in breached pouches of specific lots of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2019· Datascope Corporation

Recalled Item: Reinforced Introducer Sets Maquet 7.5 Fr. Recalled by Datascope Corporation...

The Issue: Potential for compromised sterility in breached pouches of specific lots of...

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

Class II — Potential Health HazardOngoing
DrugNovember 19, 2019· AuroMedics Pharma LLC

Recalled Item: Gabapentin Capsules Recalled by AuroMedics Pharma LLC Due to Presence of...

The Issue: Presence of Foreign Tablets/Capsules: One Losartan/HCTZ tablet was found in...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 19, 2019· Baxter Healthcare Corporation

Recalled Item: 0.9% Sodium Chloride Irrigation USP 5000 mL bags Recalled by Baxter...

The Issue: Lack of Assurance of Sterility: Product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund