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. 2,000 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,000 in last 12 months

Showing 16011620 of 46,762 recalls

Medical DeviceAugust 8, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation with the following product descriptions: 1. RayStation 9B...

The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· Philips Medical Systems Nederland B.V.

Recalled Item: IntelliSpace Cardiovascular Recalled by Philips Medical Systems Nederland...

The Issue: Software issue that results in the display of outdated information.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation with the following product descriptions: 1. RayStation 11B...

The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· Baxter Healthcare Corporation

Recalled Item: Baster Continu-Flo Solution Set Recalled by Baxter Healthcare Corporation...

The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation with the following product descriptions: 1. RayStation 7 Recalled...

The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2025· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation with the following product descriptions: 1. RayStation 6 Service...

The Issue: DICOM SOP Instance UID and Series Instance UID from RayGateway, i.e. the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2025· Flosonics Medical (R/A 1929803 ONTARIO CORP.)

Recalled Item: FloPatch FP120 Recalled by Flosonics Medical (R/A 1929803 ONTARIO CORP.) Due...

The Issue: Flowmeter patch as a human readable expiry date on the outer shipping...

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

Class III — Low RiskOngoing
DrugAugust 7, 2025· Glenmark Pharmaceuticals Inc., USA

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

The Issue: CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 7, 2025· Glenmark Pharmaceuticals Inc., USA

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

The Issue: CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 7, 2025· Glenmark Pharmaceuticals Inc., USA

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

The Issue: CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 6, 2025· Medtronic Perfusion Systems

Recalled Item: DLP Left Heart Vent Catheter Malleable body and vented connector Recalled by...

The Issue: The catheters may not retain their shape.

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

Class I — Serious Health HazardOngoing
DrugAugust 6, 2025· Westminster Pharmaceuticals LLC

Recalled Item: Metoprolol Tartrate Tablets Recalled by Westminster Pharmaceuticals LLC Due...

The Issue: CGMP Deviations: Presence of a nitrosamine, N-nitroso-metoprolol above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2025· Westminster Pharmaceuticals LLC

Recalled Item: Metoprolol Tartrate Tablets Recalled by Westminster Pharmaceuticals LLC Due...

The Issue: CGMP Deviations: Presence of a nitrosamine, N-nitroso-metoprolol above the...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2025· Glenmark Pharmaceuticals Inc., USA

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

The Issue: CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 6, 2025· Glenmark Pharmaceuticals Inc., USA

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

The Issue: CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 6, 2025· SEASPINE ORTHOPEDICS CORPORATION

Recalled Item: Reef TA Inserter Recalled by SEASPINE ORTHOPEDICS CORPORATION Due to...

The Issue: Inserter, used as part of a system with an intervertebral body fusion...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2025· Medtronic Perfusion Systems

Recalled Item: DLP Left Heart Vent Catheter Malleable body and vented connector Recalled by...

The Issue: The catheters may not retain their shape.

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 6, 2025· Olympus Corporation of the Americas

Recalled Item: ViziShot 2FLEX. Single Use Aspiration Needle. Model Number: NA-U403SX-4019....

The Issue: Potential for undetected, deformed a-traumatic tips.

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 6, 2025· Maquet Cardiovascular, LLC

Recalled Item: Vasoview Hemopro 3 Endoscopic Vessel Harvesting System Model No. C-VH-6000....

The Issue: Reports of out-of-box failures discovered during the limited launch phase....

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2025· Medtronic Perfusion Systems

Recalled Item: DLP Left Heart Vent Catheter Malleable body and vented connector Recalled by...

The Issue: The catheters may not retain their shape.

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

Class I — Serious Health HazardOngoing