Recall archive / FDA food enforcement
MyChai Chai Tea Concentrate Super. Product is packaged in the same square 0.5 gallon HDPE plastic bottles and have vo... — FDA record F-0109-2025
Reported terminated
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Aug 21, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- MyChai Chai Tea Concentrate Super. Product is packaged in the same square 0.5 gallon HDPE plastic bottles and have volumes of 68 fl oz. 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: Use 1:5 ratio 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.
- Reason
- Acidified Chai Tea product is recalled due to lack production record.
- Classification
- Class III
- Recalling firm
- My Chai Inc
- Quantity
- 3782 jugs
- Agency-reported status
- Terminated
- Source record identifier
- F-0109-2025
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Batch numbers and Expiration Dates: RC081321-MCSPR 8/13/23 RC041020-MCSPR 4/10/22 RC091321-MCSPR 9/13/23 AH042722-MCSPR 4/26/24 AH060822-MCSPR 6/7/24 RC062222-MCSPR 6/21/24 RC120822-MCSPR 12/7/24 RC121122-MCSPR 12/10/24 RC022823-MCSPR 2/27/25 RC042623-MCSPR 4/25/25 RC102023-MCSPR 10/19/26 RC121423-MCSPR 12/13/26 RC042524-MCSPR 4/24/27 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Nationwide
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
- Alaska
- Alabama
- Arkansas
- Arizona
- California
- Colorado
- Connecticut
- Delaware
- Florida
- Georgia
- Hawaii
- Iowa
- Idaho
- Illinois
- Indiana
- Kansas
- Kentucky
- Louisiana
- Massachusetts
- Maryland
- Maine
- Michigan
- Minnesota
- Missouri
- Mississippi
- Montana
- North Carolina
- North Dakota
- Nebraska
- New Hampshire
- New Jersey
- New Mexico
- Nevada
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Rhode Island
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Virginia
- Vermont
- Washington
- Wisconsin
- West Virginia
- Wyoming
Dates in the source
- Report date
- Nov 13, 2024
- Recall initiation date
- Aug 21, 2024
- Center classification date
- Nov 4, 2024
- Termination date
- Feb 3, 2026
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.