FDA recalls Vy&Tea tea sachets (15 per box) due to unapproved sibutramine. Products marketed without FDA approval may pose health risks.
Marketed Without An Approved NDA/ANDA: FDA analysis detected the presence of sibutramine.
Qikmoov is recalling Vy&Tea tea sachets (15 per box) because they contain sibutramine without FDA approval. This unapproved ingredient could cause health risks if consumed.
The FDA found sibutramine in the product, which is a drug not approved for use in the U.S. This unapproved ingredient could cause health risks if consumed.
People who purchased Vy&Tea tea sachets (15 per box) from the manufacturer in Vietnam. Those who have consumed the product are at risk.
Check for Vy&Tea tea sachets (15 per box) with Vietnamese labeling featuring a green leaf and bird. Products were sold with a best by date of 9/2021.
Look for Vy&Tea tea sachets (15 per box) with Vietnamese labeling featuring a green leaf and bird.
The FDA detected sibutramine, a drug not approved for use in the U.S., in the product.
The recall record does not specify a remedy, so no action is required beyond checking if you have the product.
No, the product contains an unapproved drug that could pose health risks if consumed.
We’ve drafted a message you can send Qikmoov to request your refund or repair — edit it as you like.
Subject: Recall D-0749-2021 — Qikmoov Qikmoov Hello, I own a Qikmoov that is covered by recall D-0749-2021 from Qikmoov. 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.
