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. 1,061 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
1,061 in last 12 months

Showing 2641–2660 of 46,762 recalls

Medical DeviceMarch 19, 2025· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Sterile Water Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: It was identified that the Medline Sterile Water and Medline Sterile 0.9%...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2025· Smith & Nephew, Inc.

Recalled Item: META-TAN LAG/COMPRESSION SCREW KIT 90MM/85MM Recalled by Smith & Nephew,...

The Issue: Integrated Lag/Compression Screw Kit has a compression screw with hexagon...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2025· Abbott Laboratories

Recalled Item: Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number:...

The Issue: When expired reagents are scanned or manually entered, the system will...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2025· Abbott Laboratories

Recalled Item: Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number:...

The Issue: When expired reagents are scanned or manually entered, the system will...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2025· Abbott Laboratories

Recalled Item: Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number:...

The Issue: When expired reagents are scanned or manually entered, the system will...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2025· Abbott Laboratories

Recalled Item: Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number:...

The Issue: When expired reagents are scanned or manually entered, the system will...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2025· Abbott Laboratories

Recalled Item: Brand Name: CELL-DYN Ruby Product Name: CELL-DYN Ruby Model/Catalog Number:...

The Issue: When expired reagents are scanned or manually entered, the system will...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2025· Beckman Coulter Inc.

Recalled Item: DxC 500 AU Clinical Chemistry Analyzer Recalled by Beckman Coulter Inc. Due...

The Issue: The reason for the recall is incorrect sample barcode identification and...

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

Class II — Potential Health HazardOngoing
DrugMarch 17, 2025· BIOCON PHARMA INC

Recalled Item: Atorvastatin Calcium Tablets USP 40 mg Recalled by BIOCON PHARMA INC Due to...

The Issue: Failed dissolution specifications: lower than specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 17, 2025· Abbott

Recalled Item: Amplatzer TorqVue LP Catheter (TVLPC) Recalled by Abbott Due to Device may...

The Issue: Device may have a small breach in the proximal end of the shaft under the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2025· Abbott

Recalled Item: Amplatzer TorqVue LP Delivery System (TVLP) Recalled by Abbott Due to Device...

The Issue: Device may have a small breach in the proximal end of the shaft under the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2025· Pro-Med Instruments Gmbh

Recalled Item: DORO¿ Easy-Connect Navigation Adaptor Recalled by Pro-Med Instruments Gmbh...

The Issue: Potential of compromised compatibility resulting in influence on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2025· Merit Medical Systems, Inc.

Recalled Item: Merit Medical Recalled by Merit Medical Systems, Inc. Due to Update to IFU...

The Issue: Update to IFU to provide additional information related to risk with device...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2025· Merit Medical Systems, Inc.

Recalled Item: Merit Medical Recalled by Merit Medical Systems, Inc. Due to Update to IFU...

The Issue: Update to IFU to provide additional information related to risk with device...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2025· ESAOTE S.P.A.

Recalled Item: Esaote Endocavity ultrasonic probe Recalled by ESAOTE S.P.A. Due to A...

The Issue: A potential weakness has been identified in the probe body, so that, in a...

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

Class II — Potential Health HazardOngoing
DrugMarch 13, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Fluphenazine Hydrochloride Tablets 2.5mg Recalled by Glenmark...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Teriflunomide Tablets Recalled by Glenmark Pharmaceuticals Inc., USA Due to...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Solifenacin Succinate Tablets 10MG Recalled by Glenmark Pharmaceuticals...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Voriconazole Tablets 200 mg Recalled by Glenmark Pharmaceuticals Inc., USA...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2025· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Propafenone Hydrochloride Extended-Release Capsules 225mg Recalled by...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund