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 1220112220 of 46,762 recalls

Medical DeviceApril 8, 2022· Radiometer Medical ApS

Recalled Item: Radiometer Recalled by Radiometer Medical ApS Due to Arterial Blood Sampler...

The Issue: Arterial Blood Sampler sterility cannot be guaranteed throughout the shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2022· Instrumentation Laboratory

Recalled Item: HemosIL ReadiPlasTin Recalled by Instrumentation Laboratory Due to Variable...

The Issue: Variable and out of specification QC results with HemosIL ReadiPlasTin. IL...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2022· Microtek Medical Inc.

Recalled Item: TMJ Arthroscopy Drape Recalled by Microtek Medical Inc. Due to Latex content...

The Issue: Latex content in product was labeled incorrectly as latex free.

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

Class II — Potential Health HazardOngoing
DrugApril 7, 2022· Mylan Pharmaceuticals Inc

Recalled Item: Rifampin for Injection Recalled by Mylan Pharmaceuticals Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: High out of specification...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 7, 2022· MALVERN PANALYTICAL LTD

Recalled Item: NanoSight NS300 Recalled by MALVERN PANALYTICAL LTD Due to Product found to...

The Issue: Product found to not comply to Class 1 Laser safety requirement.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2022· Synthes (USA) Products LLC

Recalled Item: Radial Head Replacement System Implant is a one-piece Recalled by Synthes...

The Issue: DePuy Synthes Radial Head Replacement System Contraindications added to...

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

Class II — Potential Health HazardOngoing
DrugApril 6, 2022· RemedyRepack Inc.

Recalled Item: Losartan Potassium 50 mg Tablet Recalled by RemedyRepack Inc. Due to CGMP...

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
Medical DeviceApril 6, 2022· MESA BIOTECH, INC

Recalled Item: Accula SARS-CoV-2 Test Recalled by MESA BIOTECH, INC Due to SARS-CoV-2 Test...

The Issue: SARS-CoV-2 Test has an increased potential for false positive results, which...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 6, 2022· Johnson & Johnson Surgical Vision Inc

Recalled Item: TRAY RING COVER Recalled by Johnson & Johnson Surgical Vision Inc Due to...

The Issue: Potential breach in the sterility barrier for tray ring covers.

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

Class II — Potential Health HazardOngoing
DrugApril 5, 2022· North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding

Recalled Item: PT-141 (Bremelanotide Acetate) 10 mg/mL (2 mL) Injection Recalled by North...

The Issue: Lack of Assurance of Sterility: deviations from Current Good Manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2022· North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding

Recalled Item: ARA-290 (Cibinetide Acetate) 6 mg/mL (4 mL) Injection Recalled by North...

The Issue: Lack of Assurance of Sterility: deviations from Current Good Manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2022· North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding

Recalled Item: Melanotan II 1 mg/mL (10 mL) Injection Recalled by North American Custom...

The Issue: Lack of Assurance of Sterility: deviations from Current Good Manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2022· North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding

Recalled Item: Ipamorelin Acetate/Sermorelin Acetate (1 mg/1 mg)/mL (10 mL) Injection...

The Issue: Lack of Assurance of Sterility: deviations from Current Good Manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2022· North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding

Recalled Item: Sermorelin Acetate 1 mg/mL (6 mL) Injection Recalled by North American...

The Issue: Lack of Assurance of Sterility: deviations from Current Good Manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2022· North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding

Recalled Item: BPC-157 2 mg/mL (5 mL) Injection Recalled by North American Custom...

The Issue: Lack of Assurance of Sterility: deviations from Current Good Manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2022· North American Custom Laboratories, LLC dba FarmaKeio Superior Custom Compounding

Recalled Item: LL-37 2 mg/mL (5 mL) Injection Recalled by North American Custom...

The Issue: Lack of Assurance of Sterility: deviations from Current Good Manufacturing...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 5, 2022· Aurobindo Pharma USA Inc.

Recalled Item: Cyanocobalamin Injection Recalled by Aurobindo Pharma USA Inc. Due to...

The Issue: Subpotent Drug: Out of Specification results for Assay

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 5, 2022· ARJOHUNTLEIGH POLSKA Sp. z.o.o.

Recalled Item: Sara Plus Active Floor Lift Recalled by ARJOHUNTLEIGH POLSKA Sp. z.o.o. Due...

The Issue: The device may emit smoke or ignite.

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

Class I — Serious Health HazardOngoing
DrugApril 4, 2022· Olympia Compounding Pharmacy dba Olympia Pharmacy

Recalled Item: NB-243 Recalled by Olympia Compounding Pharmacy dba Olympia Pharmacy Due to...

The Issue: CGMP Deviations: prior to October 1, 2021, environmental and personnel...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 4, 2022· Olympia Compounding Pharmacy dba Olympia Pharmacy

Recalled Item: T-50 Recalled by Olympia Compounding Pharmacy dba Olympia Pharmacy Due to...

The Issue: CGMP Deviations: prior to October 1, 2021, environmental and personnel...

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

Class II — Potential Health HazardOngoing
Refund