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Class II: temporary or reversible health riskTerminated

MyChai Chai Tea Concentrate KALI Recall

MyChai Chai Tea Concentrate KALI, 68 fl

My Chai Inc · Bend, OR

Risk level
Class II
Reported by FDA
Nov 13, 2024
Recall ID
F-0107-2025
Check your lot numberHow we source this data

Summary

My Chai recalled MyChai Chai Tea Concentrate KALI starting Aug 21, 2024. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-0107-2025 on Nov 13, 2024. Reason: Acidified Chai Tea products are recalled because pH was found above 4.1 and lack production record. Status: Terminated.

Why it was recalled

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

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 numbers, UPCs & expiration codes

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

Where it was sold

Nationwide

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-0107-2025
Classification
Class II
Status
Terminated
Recall initiated
Aug 21, 2024
FDA report date
Nov 13, 2024
Quantity
4545 jugs
Recall type
Voluntary: Firm initiated
Recalling firm
My Chai Inc

Original FDA data

Every field from FDA enforcement report F-0107-2025, exactly as published.

Show all FDA fields
City
Bend
State
OR
Status
Terminated
Country
United States
Event ID
95346
Address
1110 Se Centennial St Ste 6
Code information
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
Postal code
97702-1344
Report date
Nov 13, 2024
Product type
Food
Recall number
F-0107-2025
Classification
Class II
Recalling firm
My Chai Inc
Product quantity
4545 jugs
Termination date
Feb 3, 2026
Reason for recall
Acidified Chai Tea products are recalled because pH was found above 4.1 and lack production record.
Voluntary / mandated
Voluntary: Firm initiated
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.
Distribution pattern
Nationwide
Recall initiation date
Aug 21, 2024
Initial firm notification
Telephone
Center classification date
Nov 4, 2024

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0107-2025, published Nov 13, 2024. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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