MyChai recalls its Chai Tea Concentrate Double due to missing production records. The product was sold from 2021-2023 with specific batch dates. Consumers should check labels for batch numbers and expiration dates.
Acidified Chai Tea product is recalled due to lack production record.
MyChai is recalling its Chai Tea Concentrate Double product because it lacks production records. This recall is due to the inability to verify when the product was made, which could lead to safety issues.
The product lacks production records, meaning the manufacturer cannot confirm when the product was made. This makes it impossible to verify if the product is safe or has expired. Without knowing the production date, there is a risk of consuming an unsafe product.
Anyone who purchased MyChai Chai Tea Concentrate Double before the recall was issued. The product was sold from 2021 through early 2024, so consumers with the product should check their batch numbers.
Check the product label for batch numbers like RC060521-MCD. The product was sold in 0.5 gallon HDPE plastic bottles with expiration dates extending to 2026 for some batches.
Look for batch numbers on the label, such as RC060521-MCD, to identify if the product is part of the recall.
MyChai is recalling the product because it lacks production records, making it impossible to verify when the product was made.
Batch numbers like RC060521-MCD, RC091321-MCD, and others up to RC122123-MCD are affected.
Check the product label for batch numbers such as RC060521-MCD. The product was sold in 0.5 gallon HDPE plastic bottles with specific expiration dates.
We’ve drafted a message you can send MyChai to request your refund or repair — edit it as you like.
Subject: Recall F-0108-2025 — MyChai MyChai Hello, I own a MyChai that is covered by recall F-0108-2025 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.
