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. 2,503 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,503 in last 12 months

Showing 1144111460 of 46,762 recalls

DrugJune 10, 2022· Akorn, Inc.

Recalled Item: Calcipotriene Topical Solution Recalled by Akorn, Inc. Due to Defective...

The Issue: Defective Delivery System: Potential defect that could prevent the product...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 10, 2022· Macleods Pharma Usa Inc

Recalled Item: Losartan potassium & Hydrochlorothiazide Tablets 100 mg/25 mg Recalled by...

The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 10, 2022· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Testosterone Cypionate Injection Recalled by SUN PHARMACEUTICAL INDUSTRIES...

The Issue: Lack of Assurance of Sterility: Manufacturing deviation which was reported...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 10, 2022· Lupin Pharmaceuticals Inc.

Recalled Item: Zileuton Extended-Release Tablets Recalled by Lupin Pharmaceuticals Inc. Due...

The Issue: Failed Dissolution Specifications: Out of specification test results...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 10, 2022· Guangdong Haiou Medical Apparatus Co., Ltd

Recalled Item: Haiou Needle Retractable Safety Syringe with Needle-1ML 23G x 1 Recalled by...

The Issue: Complaints received in which needle and needle holder have detached from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2022· Guangdong Haiou Medical Apparatus Co., Ltd

Recalled Item: HAIOU Needle retractable safety syringe with needle-(1ml syringe with 25G...

The Issue: Complaints received in which needle and needle holder have detached from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Pheno Recalled by Siemens Medical Solutions USA, Inc Due to A video...

The Issue: A video signal from one of the transceivers of the Large Display may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 10, 2022· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 11B Recalled by RAYSEARCH LABORATORIES AB Due to This notice...

The Issue: This notice concerns two issues found related to the display of Linear...

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

Class II — Potential Health HazardOngoing
DrugJune 9, 2022· Green Pharmaceuticals, Inc.

Recalled Item: SnoreStop NasoSpray Recalled by Green Pharmaceuticals, Inc. Due to Microbial...

The Issue: Microbial contamination of non-sterile product: FDA laboratory analysis...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 9, 2022· Mayne Pharma Inc

Recalled Item: Clonidine Transdermal System Recalled by Mayne Pharma Inc Due to Defective...

The Issue: Defective Delivery System: Out of specification for release liner removal...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 9, 2022· Abbott Laboratories

Recalled Item: Recalled by Abbott Laboratories Due to There is a potential for falsely...

The Issue: There is a potential for falsely elevated Hemoglobin %A1c and Hemoglobin A1c...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Abbott Laboratories

Recalled Item: Hemoglobin A1c for use with Architect Recalled by Abbott Laboratories Due to...

The Issue: There is a potential for falsely elevated Hemoglobin %A1c and Hemoglobin A1c...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Abbott Laboratories

Recalled Item: Recalled by Abbott Laboratories Due to There is a potential for falsely...

The Issue: There is a potential for falsely elevated Hemoglobin %A1c and Hemoglobin A1c...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Randox Laboratories Ltd.

Recalled Item: Soluble Transferrin Receptors (STFR) Recalled by Randox Laboratories Ltd....

The Issue: A customer reported a problem with the reagent and calibrator. Randox...

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

Class III — Low RiskOngoing
Medical DeviceJune 9, 2022· Randox Laboratories Ltd.

Recalled Item: Soluble Transferrin Receptors Calibrator Series (STFR CAL) Recalled by...

The Issue: A customer reported a problem with the reagent and calibrator. Randox...

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

Class III — Low RiskOngoing
Medical DeviceJune 9, 2022· Zeltiq Aesthetics, Inc

Recalled Item: CoolMax ZELTIQ Vacuum Applicator Recalled by Zeltiq Aesthetics, Inc Due to...

The Issue: Executing a voluntary discontinuation and removal of parallel plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Zeltiq Aesthetics, Inc

Recalled Item: CoolFit ZELTIQ Vacuum Applicator Recalled by Zeltiq Aesthetics, Inc Due to...

The Issue: Executing a voluntary discontinuation and removal of parallel plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Zeltiq Aesthetics, Inc

Recalled Item: CoolCurve ZELTIQ Vaccum Applicator Recalled by Zeltiq Aesthetics, Inc Due to...

The Issue: Executing a voluntary discontinuation and removal of parallel plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Zeltiq Aesthetics, Inc

Recalled Item: CoolCurve+ ZELTIQ Vacuum Applicator Recalled by Zeltiq Aesthetics, Inc Due...

The Issue: Executing a voluntary discontinuation and removal of parallel plate...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 9, 2022· Zeltiq Aesthetics, Inc

Recalled Item: CoolCore ZELTIQ Vacuum Applicator Recalled by Zeltiq Aesthetics, Inc Due to...

The Issue: Executing a voluntary discontinuation and removal of parallel plate...

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

Class II — Potential Health HazardOngoing