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. 2,550 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,550 in last 12 months

Showing 27412760 of 46,762 recalls

DrugMarch 5, 2025· L'Oreal USA

Recalled Item: La Roche-Posay Laboratoire Dermatologique Effaclar Dermatological Acne...

The Issue: cGMP Deviations: The recall was initiated due to detected trace levels of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 5, 2025· L'Oreal USA

Recalled Item: La Roche-Posay Laboratoire Dermatologique Effaclar Duo Dual Action Acne...

The Issue: Chemical Contamination: This recall has been initiated due to detected trace...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 5, 2025· Golden State Medical Supply Inc.

Recalled Item: PRASUGREL TABLETS Recalled by Golden State Medical Supply Inc. Due to Failed...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 5, 2025· Strides Pharma, Inc.

Recalled Item: Testosterone Gel 1% Recalled by Strides Pharma, Inc. Due to Presence of...

The Issue: Presence of foreign substance: Presence of Benzene.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 5, 2025· Strides Pharma, Inc.

Recalled Item: Testosterone Gel 1% Recalled by Strides Pharma, Inc. Due to Presence of...

The Issue: Presence of foreign substance: Presence of Benzene.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 5, 2025· Rising Pharma Holding, Inc.

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Rising Pharma Holding, Inc....

The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above recommended...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 5, 2025· Tornier S.A.S.

Recalled Item: stryker Blueprint Mixed Reality Coracoid Clamp Recalled by Tornier S.A.S....

The Issue: Stryker identified an elevated complaint rate related to difficulties using...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· Tornier S.A.S.

Recalled Item: stryker Blueprint Mixed Reality Glenoid Digitizer Recalled by Tornier S.A.S....

The Issue: Stryker identified an elevated complaint rate related to difficulties using...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· Tornier S.A.S.

Recalled Item: stryker Blueprint Mixed Reality Depth Stop Pin Recalled by Tornier S.A.S....

The Issue: Stryker identified an elevated complaint rate related to difficulties using...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· Tornier S.A.S.

Recalled Item: stryker Blueprint Mixed Reality Instrument Kit Recalled by Tornier S.A.S....

The Issue: Stryker identified an elevated complaint rate related to difficulties using...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE ReNewal ENT Coblator II PROcise XP Wand Recalled by MEDLINE...

The Issue: Medline ReNewal has identified that the drip chambers of affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· Tornier S.A.S.

Recalled Item: stryker Blueprint Mixed Reality Box Base Recalled by Tornier S.A.S. Due to...

The Issue: Stryker identified an elevated complaint rate related to difficulties using...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE ReNewal Coblator II ENT Evac 70 Xtra HP Recalled by MEDLINE...

The Issue: Medline ReNewal has identified that the drip chambers of affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE ReNewal Coblator II Evac 70 Xtra Plasma Wand Recalled by MEDLINE...

The Issue: Medline ReNewal has identified that the drip chambers of affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· Tornier S.A.S.

Recalled Item: stryker Blueprint Mixed Reality BP MxR Glenoid Pin Guide PPSU + Stainless...

The Issue: Stryker identified an elevated complaint rate related to difficulties using...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· Tornier S.A.S.

Recalled Item: stryker Blueprint Mixed Reality Instrument Check Block Recalled by Tornier...

The Issue: Stryker identified an elevated complaint rate related to difficulties using...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· Tornier S.A.S.

Recalled Item: stryker HoloBlueprint Application Recalled by Tornier S.A.S. Due to Stryker...

The Issue: Stryker identified an elevated complaint rate related to difficulties using...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE ReNewal ENT Coblator II PROcise mAx Recalled by MEDLINE INDUSTRIES,...

The Issue: Medline ReNewal has identified that the drip chambers of affected devices...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2025· Tornier S.A.S.

Recalled Item: stryker Blueprint Mixed Reality Glenoid Box Lid Recalled by Tornier S.A.S....

The Issue: Stryker identified an elevated complaint rate related to difficulties using...

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

Class II — Potential Health HazardOngoing
DrugMarch 4, 2025· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Gabapentin Capsules Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...

The Issue: Cross Contamination

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

Class III — Low RiskOngoing
Refund