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. 2,506 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,506 in last 12 months

Showing 1066110680 of 46,762 recalls

DrugSeptember 20, 2022· QuVa Pharma, Inc.

Recalled Item: oxyTOCIN 30 Units/500 mL (0.06 Units/mL) added to 0.9% Sodium Chloride...

The Issue: Incorrect Product Formulation: Oxytocin 30 units was added to an IV bag of...

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 20, 2022· Medtronic MiniMed

Recalled Item: Insulin Pump/Model: MiniMed 620G/ MMT-1750 MiniMed 640G/ MMT-1711 Recalled...

The Issue: Medtronic identified a cybersecurity vulnerability in the MiniMed 600 series...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2022· Medtronic MiniMed

Recalled Item: Insulin Pump/Model: MiniMed 630G/ MMT-1715 Recalled by Medtronic MiniMed Due...

The Issue: Medtronic identified a cybersecurity vulnerability in the MiniMed 600 series...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2022· Intuitive Surgical, Inc.

Recalled Item: da Vinci X (IS4200) and Xi (IS4000) systems Recalled by Intuitive Surgical,...

The Issue: Inadvertent energy delivery from surgical system instrument if 1) Force...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2022· Angiodynamics, Inc.

Recalled Item: Vortex MP Port Titanium Low Profile Implanted Port with 5F Recalled by...

The Issue: Printed Instructions for Use (IFU) not shipped with device. The Instructions...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: ARTIS pheno Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...

The Issue: Siemens has become aware of three potential software issues with ARTIS pheno...

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

Class II — Potential Health HazardOngoing
DrugSeptember 19, 2022· UNICHEM PHARMACEUTICALS USA INC

Recalled Item: Clonidine Hydrochloride Tablets Recalled by UNICHEM PHARMACEUTICALS USA INC...

The Issue: Product mix-up:0.2 mg strength Clonidine Hydrochloride Tablets, USP in a...

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

Class III — Low RiskOngoing
Refund
FoodSeptember 19, 2022· Secrets Of The Tribe

Recalled Item: Indian Gooseberry Alcohol-Free Extract Recalled by Secrets Of The Tribe Due...

The Issue: Product has elevated level of lead.

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 19, 2022· Secrets Of The Tribe

Recalled Item: Amla Alcohol-Free Extract Recalled by Secrets Of The Tribe Due to Product...

The Issue: Product has elevated level of lead.

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 19, 2022· World Variety Produce Inc dba Melissa's

Recalled Item: Dutch Red Potatoes with Dijon Mustard Sauce. NET WT. 1 Recalled by World...

The Issue: Dutch Red Potatoes were packed with a Dijon Mustard Sauce packet that did...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceSeptember 19, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Lithium (Li) Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: Potential for falsely elevated LITH_2 and Li results on the Atellica CH 930...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Lithium_2 (LITH_2) Recalled by Siemens Healthcare Diagnostics,...

The Issue: Potential for falsely elevated LITH_2 and Li results on the Atellica CH 930...

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

Class II — Potential Health HazardOngoing
DrugSeptember 16, 2022· Novartis Pharmaceuticals Corporation

Recalled Item: Neoral soft gelatin capsules (cyclosporine capsules Recalled by Novartis...

The Issue: CGMP deviations: Out of specification results obtained during routine...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 16, 2022· ALMIRALL, LLC

Recalled Item: Xolegel (ketoconazole) gel 2% Recalled by ALMIRALL, LLC Due to Failed...

The Issue: Failed Viscosity specification: Slightly higher OOS results obtained for...

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

Class III — Low RiskOngoing
Refund
FoodSeptember 16, 2022· Seeking Health LLC

Recalled Item: Seeking Health brand Optimal Multivitamin Chewable Dietary Supplement...

The Issue: The product label claim for copper is 0.5mg, but third-party lab results...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 16, 2022· Fresenius Kabi USA, LLC

Recalled Item: LVP software of the Ivenix Infusion System (IIS) Recalled by Fresenius Kabi...

The Issue: Retroactively reported correction from 2022: A software defect may cause an...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2022· International Medical Industries, Inc.

Recalled Item: Prep-Fill Guarded Luer Connector (GLC): a. Part Number 57-400 Recalled by...

The Issue: Blister package had an unsealed edge compromising sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2022· Olympus Corporation of the Americas

Recalled Item: Berkeley VC-10 Vacuum Curettage System Recalled by Olympus Corporation of...

The Issue: Update to the Instruction for Use (IFU): Olympus is adding a new warning...

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

Class II — Potential Health HazardOngoing
DrugSeptember 15, 2022· CIPLA

Recalled Item: Budesonide Inhalation Suspension 0.25mg/2mL Recalled by CIPLA Due to Lack of...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 15, 2022· RemedyRepack Inc.

Recalled Item: Lisinopril 10 mg tablets Recalled by RemedyRepack Inc. Due to Foreign Object...

The Issue: Presence of Foreign Substance: Foreign material (metal piece) embedded in...

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

Class II — Potential Health HazardOngoing
Refund