MyChai recalls 68 fl oz chai tea concentrate KALI due to pH above 4.1 and missing production records. Consumers should check batch numbers and expiration dates for affected lots.
Acidified Chai Tea products are recalled because pH was found above 4.1 and lack production record.
MyChai is recalling its KALI chai tea concentrate (68 fl oz) because the product's pH level is too high (above 4.1) and lacks proper production records. This could pose a food safety risk, though the recall does not specify serious injury potential.
The chai tea concentrate has a pH level above 4.1, which is too acidic for safe food handling. The product also lacks production records, making it difficult to verify its safety. This could lead to foodborne illness or contamination.
Anyone who purchased MyChai KALI chai tea concentrate between August 2021 and December 2023. The risk is higher for people with sensitive stomachs or those who consume large quantities.
Check the batch number on the label, which starts with RC followed by a date (e.g., RC082121-MCK). The product was sold between August 2021 and December 2023 with expiration dates up to 3 years from production.
Look for batch numbers on the label starting with RC followed by a date (e.g., RC082121-MCK).
Reach out to MyChai at 1110 SE Centennial St. Suite 6, Bend, OR 97702 for assistance with the recall.
The product has a pH level above 4.1 and lacks proper production records, which could pose a food safety risk.
Check the batch number on the label, which starts with RC followed by a date (e.g., RC082121-MCK). The product was sold between August 2021 and December 2023.
Contact MyChai at 1110 SE Centennial St. Suite 6, Bend, OR 97702 for assistance with the recall.
We’ve drafted a message you can send MyChai to request your refund or repair — edit it as you like.
Subject: Recall F-0107-2025 — MyChai MyChai Hello, I own a MyChai that is covered by recall F-0107-2025 from MyChai. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
