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. 2,480 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,480 in last 12 months

Showing 1472114740 of 46,762 recalls

Medical DeviceMay 14, 2021· DeRoyal Industries Inc

Recalled Item: DeRoyal Heart Cath Procedure Pack Recalled by DeRoyal Industries Inc Due to...

The Issue: DeRoyal manufactured certain lots of surgical procedure pack products using...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 14, 2021· DeRoyal Industries Inc

Recalled Item: DeRoyal Pacemaker Tray Pgybk Recalled by DeRoyal Industries Inc Due to...

The Issue: DeRoyal manufactured certain lots of surgical procedure pack products using...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 13, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1300 Analyzer - multi-component system for in vitro Recalled by...

The Issue: Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM 1600 Analyzer- multi-component system for in vitro diagnostic...

The Issue: Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 13, 2021· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH 930 Analyzer - multi-component system for in vitro Recalled by...

The Issue: Valves used on the Atellica CH 930, Atellica IM 1300 and Atellica IM 1600...

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

Class II — Potential Health HazardOngoing
DrugMay 12, 2021· American Health Packaging

Recalled Item: Sirolimus Tablets 1 mg Recalled by American Health Packaging Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugMay 12, 2021· Global Sanitizers LLC

Recalled Item: MEDICALLY MINDED Hand Sanitizer Gel Recalled by Global Sanitizers LLC Due to...

The Issue: CGMP Deviations: lots and products of hand sanitizer are being recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 12, 2021· Global Sanitizers LLC

Recalled Item: MEDICALLY MINDED Hand Sanitizer Gel Recalled by Global Sanitizers LLC Due to...

The Issue: Chemical Contamination: FDA analysis found 1 lot of MEDICALLY MINDED Hand...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 12, 2021· Global Sanitizers LLC

Recalled Item: MEDICALLY MINDED Hand Sanitizer Gel Recalled by Global Sanitizers LLC Due to...

The Issue: CGMP Deviations: lots and products of hand sanitizer are being recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 12, 2021· Global Sanitizers LLC

Recalled Item: MEDICALLY MINDED Hand Sanitizer Gel Recalled by Global Sanitizers LLC Due to...

The Issue: CGMP Deviations: lots and products of hand sanitizer are being recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 12, 2021· Global Sanitizers LLC

Recalled Item: MEDICALLY MINDED ANTIMICROBIAL Hand Sanitizer Gel with Aloe Vera Recalled by...

The Issue: CGMP Deviations: lots and products of hand sanitizer are being recalled...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 12, 2021· Global Sanitizers LLC

Recalled Item: MEDICALLY MINDED Hand Sanitizer Gel Recalled by Global Sanitizers LLC Due to...

The Issue: Chemical Contamination: FDA analysis found 1 lot of MEDICALLY MINDED Hand...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 12, 2021· CardioQuip, LLC

Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to Labeling does not include...

The Issue: Labeling does not include guidance for proper water-quality maintenance and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· CardioQuip, LLC

Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to Labeling does not include...

The Issue: Labeling does not include guidance for proper water-quality maintenance and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· CardioQuip, LLC

Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to Labeling does not include...

The Issue: Labeling does not include guidance for proper water-quality maintenance and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· CardioQuip, LLC

Recalled Item: CardioQuip Recalled by CardioQuip, LLC Due to Labeling does not include...

The Issue: Labeling does not include guidance for proper water-quality maintenance and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: Prime Fifth Wheel Stretcher-stretcher may be used for minor procedures...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: Proform- support surface is used to assist in the prevention Recalled by...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: Prime Big Wheel Stretcher-used as a short-term outpatient clinical...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2021· Stryker Medical Division of Stryker Corporation

Recalled Item: S3 MedSurg Bed - intended to support and transport patients Recalled by...

The Issue: Medical devices intended for use in a healthcare facility were distributed...

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

Class II — Potential Health HazardOngoing