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 1230112320 of 46,762 recalls

DrugMarch 29, 2022· Teva Pharmaceuticals USA Inc

Recalled Item: IDArubicin Hydrochloride Injection USP 5gm/5mL (1mg/mL) for intravenous use...

The Issue: Presence of Particulate Matter: Product was found to contain silica and iron...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 28, 2022· Preferred Pharmaceuticals, Inc.

Recalled Item: Preferred Pharmaceuticals Recalled by Preferred Pharmaceuticals, Inc. Due to...

The Issue: Out of specification results observed in dissolution during long term...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 28, 2022· Medminder Systems, Inc.

Recalled Item: MedMinder Medication Dispenser- Intended to serve as a medication reminder...

The Issue: Discontinuation of the Emergency Alert watch or pendant will no longer...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2022· Stryker GmbH

Recalled Item: Smart Toe II Intramedullary Arthrodesis Implant Recalled by Stryker GmbH Due...

The Issue: The nickel-sensitivity statement on the outer carton may be partially...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2022· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD Anti-Kappa PE (Cat. No. 346587) is an analyte specific Recalled by...

The Issue: Anti-Kappa APC & Anti-Kappa PE analyte reagents may exhibit uncharacteristic...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2022· Becton, Dickinson and Company, BD Biosciences

Recalled Item: BD Anti-Kappa APC (Cat. No. 341098) is an analyte specific Recalled by...

The Issue: Anti-Kappa APC & Anti-Kappa PE analyte reagents may exhibit uncharacteristic...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2022· Ortho-Clinical Diagnostics, Inc

Recalled Item: VITROS Immunodiagnostic Products LH Reagent Pack Product Code: 1350198...

The Issue: Falsely high or delayed patient and QC results may occur due to low end...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2022· Ortho-Clinical Diagnostics, Inc

Recalled Item: VITROS Immunodiagnostic Products Prolactin Reagent Pack Product Code:...

The Issue: Falsely high or delayed patient and QC results may occur due to low end...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2022· Ortho-Clinical Diagnostics, Inc

Recalled Item: VITROS Immunodiagnostic Products FSH Reagent Pack- IVD 1931922 Recalled by...

The Issue: Falsely high or delayed patient and QC results may occur due to low end...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2022· Olympus Corporation of the Americas

Recalled Item: Olympus Uretero-reno videoscope Recalled by Olympus Corporation of the...

The Issue: The bending section of the URF-V2 may crack, resulting in an abnormal shape...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2022· Arthrex, Inc.

Recalled Item: K-Wire Recalled by Arthrex, Inc. Due to Products do not meet length and...

The Issue: Products do not meet length and diameter specifications.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2022· Medtronic formerly Covidien

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Medtronic formerly...

The Issue: The audible alarm may not sound and/or the omni-directional LED visual alarm...

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

Class I — Serious Health HazardOngoing
DrugMarch 24, 2022· Preferred Pharmaceuticals, Inc.

Recalled Item: Diclofenac Sodium Topical Solution 1.5% w/w Recalled by Preferred...

The Issue: CGMP Deviations: all products within expiry are being recalled because the...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 24, 2022· Wilton Industries Inc

Recalled Item: Wilton Ready to Build Chocolate Cookie Bunny Hutch Kit Recalled by Wilton...

The Issue: Milk is missing from the product's allergen Contains statement

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 24, 2022· Microbiologics Inc

Recalled Item: Inactivated macrolide and quinolone-resistant Mycoplasma genitalium Recalled...

The Issue: QC process was not adequate for the specification range.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2022· Abbott

Recalled Item: Abbott SE TactiCath Sensor Enabled Contact Force Ablation Catheter Recalled...

The Issue: Devices were manufactured with a "First Use Date" preprogrammed in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2022· Abbott

Recalled Item: Abbott SE TactiCath Sensor Enabled Contact Force Ablation Catheter Recalled...

The Issue: Devices were manufactured with a "First Use Date" preprogrammed in the...

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

Class II — Potential Health HazardOngoing
DrugMarch 23, 2022· Drug Depot, Inc., dba APS Pharmacy

Recalled Item: TESTOSTERONE CYPIONATE/ ANASTROZOLE *GS* OIL (10ML) 200MG/0.5MG/ML Recalled...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 23, 2022· Drug Depot, Inc., dba APS Pharmacy

Recalled Item: GONADORELIN (5ML) 0.2 MG/ML INJECTABLE Recalled by Drug Depot, Inc., dba APS...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 23, 2022· Drug Depot, Inc., dba APS Pharmacy

Recalled Item: TESTOSTERONE CYPIONATE/ DHEA *GS* 200/10MG/ML Injectable Recalled by Drug...

The Issue: Lack of sterility assurance.

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

Class II — Potential Health HazardOngoing
Refund