Recall
FDAFoodAugust 21, 2024

My Chai Inc — MyChai Chai Tea Concentrate Original. Product is packaged in plastic (HDPE) 1/2gallon bottle, cap has a foil liner that is induction sealed during the bottling process. Shelf stable 3 ye

⚠️ Acidified Chai Tea products are recalled because pH was found above 4.1 and lack production record.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Food
Published
August 21, 2024

Nationwide

What's affected?

Product
MyChai Chai Tea Concentrate Original. Product is packaged in plastic (HDPE) 1/2gallon bottle, cap has a foil liner that is induction sealed during the bottling process. Shelf stable 3 year expiration from date of manufacture. Ingredients: Water, Sugar, Organic Black Tea, Organic Spices, Molasses, Vanilla Extract, Citric Acid, Natural Flavors. Made by: MyChai, Inc. 1110 SE Centennial St. Suite 6, Bend, OR 97702 USAGE: Please use 1:1 with milk or soy. Up until fall of 2023, expiration dates were 2 years from the date of production. In the fall of 2023 expiration dates were extended an additional year to 3 years from the production date.
Lot code
Batch numbers and Expiration Dates: RC080321-MCO 8/3/23 RC110121-MCO 11/1/23 RC120521-MCO 12/5/23 RC020322-MCO 2/3/24 AH050322-MCO 5/2/24 AH061022-MCO 6/9/24 RC081222-MCO 8/11/24 RC122120-MCO 12/21/22 RC012320-MCO 1/22/22 RC111822-MCO 11/17/24 RC112322-MCO 11/22/24 RC120322-MCO 12/2/24 RC120922-MCO 12/8/24 RC022023-MCO 2/19/25 RC060123-MCO 5/31/25 RC101923-MCO 110/18/26 RC112823-MCO 11/27/26 RC122023-MCO 12/19/26 RC052124-MCO 5/21/27

Additional details

Batch numbers and Expiration Dates: RC080321-MCO 8/3/23 RC110121-MCO 11/1/23 RC120521-MCO 12/5/23 RC020322-MCO 2/3/24 AH050322-MCO 5/2/24 AH061022-MCO 6/9/24 RC081222-MCO 8/11/24 RC122120-MCO 12/21/22 RC012320-MCO 1/22/22 RC111822-MCO 11/17/24 RC112322-MCO 11/22/24 RC120322-MCO 12/2/24 RC120922-MCO 12/8/24 RC022023-MCO 2/19/25 RC060123-MCO 5/31/25 RC101923-MCO 110/18/26 RC112823-MCO 11/27/26 RC122023-MCO 12/19/26 RC052124-MCO 5/21/27

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 19,061 jugs.

View original FDA notice →

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