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. 967 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
967 in last 12 months

Showing 25241–25260 of 46,762 recalls

DrugFebruary 9, 2018· American Pharmaceutical Ingredients LLC

Recalled Item: Sildenafil Citrate USP for prescription compounding Recalled by American...

The Issue: CGMP Deviations: Lack of stability data and controls to support the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2018· American Pharmaceutical Ingredients LLC

Recalled Item: Duloxetine HCl USP for prescription compounding Recalled by American...

The Issue: CGMP Deviations: Lack of stability data and controls to support the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2018· American Pharmaceutical Ingredients LLC

Recalled Item: Estradiol USP (Micronized) (Yam) for prescription compounding Recalled by...

The Issue: CGMP Deviations: Lack of stability data and controls to support the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2018· American Pharmaceutical Ingredients LLC

Recalled Item: Tadalafil USP (Monohydrate) for prescription compounding Recalled by...

The Issue: CGMP Deviations: Lack of stability data and controls to support the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2018· American Pharmaceutical Ingredients LLC

Recalled Item: Cyclobenzaprine HCl USP for prescription compounding Recalled by American...

The Issue: CGMP Deviations: Lack of stability data and controls to support the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2018· American Pharmaceutical Ingredients LLC

Recalled Item: Baclofen USP (Micronized) for prescription compounding Recalled by American...

The Issue: CGMP Deviations: Lack of stability data and controls to support the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2018· American Pharmaceutical Ingredients LLC

Recalled Item: Testosterone Cypionate USP (Micronized) for prescription compounding...

The Issue: CGMP Deviations: Lack of stability data and controls to support the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2018· American Pharmaceutical Ingredients LLC

Recalled Item: Calcipotriene BP (Monohydrate) for prescription compounding Recalled by...

The Issue: CGMP Deviations: Lack of stability data and controls to support the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2018· American Pharmaceutical Ingredients LLC

Recalled Item: Nifedipine USP for prescription compounding Recalled by American...

The Issue: CGMP Deviations: Lack of stability data and controls to support the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2018· American Pharmaceutical Ingredients LLC

Recalled Item: Imiquimod USP for prescription compounding Recalled by American...

The Issue: CGMP Deviations: Lack of stability data and controls to support the...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 9, 2018· Apace KY LLC

Recalled Item: Acyclovir Tablets Recalled by Apace KY LLC Due to Presence of Foreign...

The Issue: Presence of Foreign Tablet/Capsule; cartons labeled to contain Acyclovir...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 9, 2018· Divinity Product Distribution LLC

Recalled Item: Kratom powder labeled in the following ways 1) Enhance Your Life Recalled by...

The Issue: The firm's dietary supplement products contain kratom (Mitragyna speciosa),...

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 9, 2018· Divinity Product Distribution LLC

Recalled Item: Kratom capsules labeled in the following ways: 1) Divinity Kratom Recalled...

The Issue: The firm's dietary supplement products contain kratom (Mitragyna speciosa),...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 - Model no. 728231 Recalled by Philips Medical Systems...

The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE isp Implantable Port With Smooth Septum and Attachable...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE isp with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 6 Slice (Air) - Model no. 728256 Recalled by Philips Medical...

The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity CT - Model no. 728326 Recalled by Philips Medical Systems...

The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...

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

Class II — Potential Health HazardOngoing