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. 2,353 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,353 in last 12 months

Showing 2442124440 of 46,762 recalls

DrugMay 25, 2018· Shadow Holdings DBA Bocchi Labs

Recalled Item: Acne Shave Post-Shave Moisturizer (salicylic acid) Recalled by Shadow...

The Issue: CGMP Deviations: products may be contaminated with bacteria.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 25, 2018· Shadow Holdings DBA Bocchi Labs

Recalled Item: Acne Shave (salicylic acid) Shave Cream Acne Shield Recalled by Shadow...

The Issue: CGMP Deviations: products may be contaminated with bacteria.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 25, 2018· Dean Foods, Inc.

Recalled Item: Baskin Robbins Mint Chocolate Chip Recalled by Dean Foods, Inc. Due to...

The Issue: Product may contain unlabeled coconut.

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 24, 2018· Allergan, PLC.

Recalled Item: Allergan Taytulla Softgel Capsules Recalled by Allergan, PLC. Due to...

The Issue: Contraceptive Tablets Out of Sequence.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 24, 2018· Beckman Coulter Inc.

Recalled Item: Software Package Recalled by Beckman Coulter Inc. Due to Sorting-Drive...

The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...

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

Class III — Low RiskOngoing
Medical DeviceMay 24, 2018· Beckman Coulter Inc.

Recalled Item: Sorting-Drive Product Part Recalled by Beckman Coulter Inc. Due to...

The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...

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

Class III — Low RiskOngoing
Medical DeviceMay 24, 2018· Beckman Coulter Inc.

Recalled Item: Intelligent Peri-Analytical Workstation (HW+SW) Recalled by Beckman Coulter...

The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...

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

Class III — Low RiskOngoing
Medical DeviceMay 24, 2018· Beckman Coulter Inc.

Recalled Item: Sorting-Drive Professional Part Recalled by Beckman Coulter Inc. Due to...

The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...

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

Class III — Low RiskOngoing
Medical DeviceMay 24, 2018· Beckman Coulter Inc.

Recalled Item: Software Package Recalled by Beckman Coulter Inc. Due to Sorting-Drive...

The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...

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

Class III — Low RiskOngoing
Medical DeviceMay 24, 2018· Beckman Coulter Inc.

Recalled Item: Software Package Recalled by Beckman Coulter Inc. Due to Sorting-Drive...

The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...

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

Class III — Low RiskOngoing
Medical DeviceMay 24, 2018· Beckman Coulter Inc.

Recalled Item: Software Package Recalled by Beckman Coulter Inc. Due to Sorting-Drive...

The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...

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

Class III — Low RiskOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: Optima CT 540 Recalled by GE Healthcare, LLC Due to Some CT and CT/PET...

The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: CT Goldseal Optima CT 600 Recalled by GE Healthcare, LLC Due to Some CT and...

The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: Revolution EVO 3.6 Recalled by GE Healthcare, LLC Due to Some CT and CT/PET...

The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: Discovery MI Digital Ready Recalled by GE Healthcare, LLC Due to DIGITAL...

The Issue: DIGITAL ReadyCT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: Discovery IQ 2.0 20cm Recalled by GE Healthcare, LLC Due to Some CT and...

The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: Optima CT 520 Recalled by GE Healthcare, LLC Due to Some CT and CT/PET...

The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: Revolution CT 160 1.5D STD WAUK Recalled by GE Healthcare, LLC Due to Some...

The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: Discovery MI Recalled by GE Healthcare, LLC Due to Some CT and CT/PET...

The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: Discovery RT labeled as: a. MID BJG Recalled by GE Healthcare, LLC Due to...

The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing