MyChai Chai Tea Concentrate KALI, 68 fl. oz. Product is packaged in plastic (HDPE) 1/2gallon bottle, cap has a foil line
Summary
The FDA issued a Class II for MyChai Chai Tea Concentrate KALI, 68 fl. oz. Product is packaged in plastic (HDP by My Chai Inc. Reason: Acidified Chai Tea products are recalled because pH was found above 4.1 and lack production record..
Details
Source
Food Recall
External ID
F-0107-2025
Action Date
2024-11-13
Status
Terminated
Category
food
Product Description
MyChai Chai Tea Concentrate KALI, 68 fl. oz. 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 Extract, Organic Spices, Molasses, Vanilla Extract, Natural Flavors, Citric Acid. Made by: MyChai, Inc. 1110 SE Centennial St. Suite 6, Bend, OR 97702. USAGE: Mix 1 part chai to 5 parts 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 Info: Batch numbers and Expiration Dates: RC082121-MCK 8/21/23 RC041720-MCK 4/17/22 RC110121-MCK 11/1/23 RC113021-MCK 11/30/23 RC101822-MCK 10/17/24 RC120122-MCK 11/30/24 RC011223-MCK 1/11/25 RC042623-MCK 4/25/25 RC052623-MCK 5/25/25 RC071023-MCK 7/9/26 RC120523-MCK 12/4/26
Quantity Affected: 4545 jugs
Reason for Recall
Acidified Chai Tea products are recalled because pH was found above 4.1 and lack production record.
Distribution
Nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2024-08-21
Company
Bend, OR
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 55 food recalls issued in the same week, part of 204 food-related FDA actions this month.
My Chai Inc has 14 FDA actions in our database, including 14 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (My Chai Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does My Chai Inc have FDA actions?
My Chai Inc has 14 FDA actions in our database, including 14 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0107-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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