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. 2,503 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,503 in last 12 months

Showing 1218112200 of 46,762 recalls

DrugApril 13, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Kinevac (Sincalide for Injection) Recalled by Mckesson Medical-Surgical Inc....

The Issue: cGMP deviations: Temperature abuse

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 13, 2022· Mckesson Medical-Surgical Inc. Corporate Office

Recalled Item: Ipratropium Bromide 0.5 mg and Albuterol Sulfate 3 mg Inhalation Recalled by...

The Issue: cGMP deviations: Temperature abuse

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 13, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1300 Analyzer - automated Recalled by Siemens Healthcare...

The Issue: Lots incompatible with Test Definition (TDef) Version 1.4, potentially lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2022· Medacta Usa Inc

Recalled Item: GMK Efficiency - GMK Sphere CR Insert Instrument Set Size 1 Recalled by...

The Issue: A Size 2 trial baseplate was assembled with Size 1 instrument sets.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1600 Analyzer - automated Recalled by Siemens Healthcare...

The Issue: Lots incompatible with Test Definition (TDef) Version 1.4, potentially lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2022· Getinge Usa Sales Inc

Recalled Item: Getinge CM320 WUWD Series Washer Disinfector-For use as a multi-chamber...

The Issue: Verification of installation not documented or may be incomplete, could...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Sensis Recalled by Siemens Medical Solutions USA, Inc Due to Siemens has...

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

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2022· Northgate Technologies, Inc.

Recalled Item: AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe...

The Issue: Product labeled incorrectly.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2022· Getinge Usa Sales Inc

Recalled Item: Getinge CM320-2 CHAMBER WU Series Washer Disinfector- For Use as Recalled by...

The Issue: Verification of installation not documented or may be incomplete, could...

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

Class II — Potential Health HazardOngoing
DrugApril 12, 2022· Mylan Pharmaceuticals Inc

Recalled Item: Insulin Glargine (insulin glargine-yfgn) Injection Recalled by Mylan...

The Issue: Labeling: Missing label on the vial

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 12, 2022· Preferred Pharmaceuticals, Inc.

Recalled Item: Losartan Potassium Tab. USP 50mg Recalled by Preferred Pharmaceuticals, Inc....

The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 12, 2022· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Crome Models loaded with CareLink SmartSync Device Manager application...

The Issue: Telemetry error that may occur with Medtronic Cobalt and Crome implantable...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 12, 2022· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: Cobalt Models loaded with CareLink SmartSync Device Manager application...

The Issue: Telemetry error that may occur with Medtronic Cobalt and Crome implantable...

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

Class II — Potential Health HazardOngoing
DrugApril 11, 2022· Torrent Pharma Inc

Recalled Item: Pantoprazole Sodium Delayed-Release Tablets Recalled by Torrent Pharma Inc...

The Issue: CGMP deviations: tablets cracking

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 11, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis icono biplane -angiography systems developed for single and biplane...

The Issue: if the protective earth is interrupted and an additional fault leads to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis icono floor-angiography systems developed for single and biplane...

The Issue: if the protective earth is interrupted and an additional fault leads to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2022· Umano Medical, Inc.

Recalled Item: AC-powered adjustable medical beds with built-in electric DC actuators and...

The Issue: There is a potential hazard of uninterrupted motion of the Motorized Wheel...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2022· Umano Medical, Inc.

Recalled Item: AC-powered adjustable medical beds with built-in electric DC actuators and...

The Issue: There is a potential hazard of uninterrupted motion of the Motorized Wheel...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2022· TELEFLEX MEDICAL INC

Recalled Item: (1) Gibeck Humid-Vent 2S Flex DC Recalled by TELEFLEX MEDICAL INC Due to...

The Issue: Reports received of torn corrugated breathing tubes.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 11, 2022· TELEFLEX MEDICAL INC

Recalled Item: (1) Teleflex Flex tube Recalled by TELEFLEX MEDICAL INC Due to Reports...

The Issue: Reports received of torn corrugated breathing tubes.

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

Class II — Potential Health HazardOngoing