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. 2,534 recalls have been distributed to Alaska in the last 12 months.

46,762 total recalls
2,534 in last 12 months

Showing 43814400 of 46,762 recalls

FoodAugust 21, 2024· My Chai Inc

Recalled Item: MyChai Chai Tea Concentrate Super. Product is packaged in the Recalled by My...

The Issue: Acidified Chai Tea product is recalled due to lack production record.

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

Class III — Low RiskOngoing
Refund
FoodAugust 21, 2024· My Chai Inc

Recalled Item: MyChai Chai Tea Concentrate Original. Product is packaged in plastic...

The Issue: Acidified Chai Tea products are recalled because pH was found above 4.1 and...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 21, 2024· My Chai Inc

Recalled Item: MyChai Chai Tea Concentrate Original Double. Product is packaged in Recalled...

The Issue: Acidified Chai Tea product is recalled due to lack production record.

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

Class III — Low RiskOngoing
Refund
FoodAugust 21, 2024· My Chai Inc

Recalled Item: MySyrup Sugar Free Peppermint Syrup. Product is packaged in the Recalled by...

The Issue: Acidified product is recalled due to lack production record.

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

Class III — Low RiskOngoing
Refund
FoodAugust 21, 2024· My Chai Inc

Recalled Item: MySyrup Sugar Free Almond Syrup. Product is packaged in the Recalled by My...

The Issue: Acidified product is recalled due to lack production record.

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

Class III — Low RiskOngoing
Refund
FoodAugust 21, 2024· My Chai Inc

Recalled Item: MyChai Chai Tea Concentrate KALI Recalled by My Chai Inc Due to Acidified...

The Issue: Acidified Chai Tea products are recalled because pH was found above 4.1 and...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 21, 2024· My Chai Inc

Recalled Item: MySyrup Sugar Free Raspberry Syrup. Product is packaged in the Recalled by...

The Issue: Acidified product is recalled due to lack production record.

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

Class III — Low RiskOngoing
Refund
FoodAugust 21, 2024· My Chai Inc

Recalled Item: MyChai Chai Tea Concentrate Double. Product is packaged in the Recalled by...

The Issue: Acidified Chai Tea product is recalled due to lack production record.

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

Class III — Low RiskOngoing
Refund
FoodAugust 21, 2024· My Chai Inc

Recalled Item: MySyrup Sugar Free Coconut Syrup. Product is packaged in the Recalled by My...

The Issue: Acidified product is recalled due to lack production record.

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

Class III — Low RiskOngoing
Refund
FoodAugust 21, 2024· My Chai Inc

Recalled Item: MySyrup Sugar Free Hazelnut Syrup. Product is packaged in the Recalled by My...

The Issue: Acidified product is recalled due to lack production record.

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

Class III — Low RiskOngoing
Refund
FoodAugust 21, 2024· Unilever North America Supply Chain Company, LLC

Recalled Item: Popsicle Jolly Rancher Frozen Confection Pop Net Wt 2.71 FL Recalled by...

The Issue: Undeclared milk

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 21, 2024· Lupin Pharmaceuticals Inc.

Recalled Item: Cefixime for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...

The Issue: Subpotent Drug- An out of specification ( OOS ) result observed in assay...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 21, 2024· Intuitive Surgical, Inc.

Recalled Item: da Vinci 5 Recalled by Intuitive Surgical, Inc. Due to Surgical system Error...

The Issue: Surgical system Error 23062 due to connector1) Partially damaged "Potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2024· Olympus Corporation of the Americas

Recalled Item: Olympus Gastrointestinal Videoscope Recalled by Olympus Corporation of the...

The Issue: It was discovered during device performance testing that the CCD imaging...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2024· CHANGE HEALTHCARE CANADA COMPANY

Recalled Item: Horizon Cardiology Hemo. Version 12.2. Recalled by CHANGE HEALTHCARE CANADA...

The Issue: A potential issue has been identified in Change Healthcare Cardiology Hemo...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2024· XTANT Medical Holdings, Inc

Recalled Item: Cortera Spinal Fixation System Screw Recalled by XTANT Medical Holdings, Inc...

The Issue: Spinal fixation system implant screws marked "DNI" are not intended to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2024· CHANGE HEALTHCARE CANADA COMPANY

Recalled Item: Change Healthcare Cardiology Hemo. Versions 14.2 Recalled by CHANGE...

The Issue: A potential issue has been identified in Change Healthcare Cardiology Hemo...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2024· CHANGE HEALTHCARE CANADA COMPANY

Recalled Item: McKesson Cardiology Hemo. Versions 13.0 Recalled by CHANGE HEALTHCARE CANADA...

The Issue: A potential issue has been identified in Change Healthcare Cardiology Hemo...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2024· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur aTPO Assay Recalled by Siemens Healthcare Diagnostics, Inc....

The Issue: Positive bias in patient results at and below the cut-off of 60 U/mL with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2024· Percussionaire Corporation

Recalled Item: Percussionaire Recalled by Percussionaire Corporation Due to Updated...

The Issue: Updated labeling to ensure that blue cap on in-line valve is removed, prior...

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

Class I — Serious Health HazardOngoing