PepsiCo recalls 24-pack of Lipton Diet Green Tea Citrus bottles due to undeclared aspartame and missing phenylketonurics warning. Consumers should check UPC #0-12000-01722-3.
Undeclared aspartame and lack of Phenylketonurics warning on immediate container (16.9fl.oz. bottle)
PepsiCo is recalling 24-pack of Lipton Diet Green Tea Citrus bottles because they contain undeclared aspartame and lack a phenylketonurics warning label. This affects people with phenylketonuria (PKU) who need to avoid aspartame.
The bottles contain aspartame without a clear warning for individuals with PKU. Aspartame is a sweetener that can cause health issues if consumed by people with PKU who require strict avoidance. The product lacks the necessary label to alert these consumers.
People with phenylketonuria (PKU) who need to avoid aspartame are most at risk. The recall applies to consumers who purchased the 24-pack of Lipton Diet Green Tea Citrus bottles with the specific UPC code.
Check for the UPC code 0-12000-01722-3 on the bottle. The product is a 24-pack of 16.9 fl oz Lipton Diet Green Tea Citrus bottles with a best by date of September 17, 2023.
Look for the UPC code 0-12000-01722-3 on the bottle to confirm it's part of the recall.
The product contains aspartame without a phenylketonurics warning label, which poses a risk for people with phenylketonuria (PKU).
The recall record does not specify a remedy, so consumers should check the product details and contact PepsiCo if needed.
Check for the UPC code 0-12000-01722-3 on the bottle, which is part of a 24-pack of Lipton Diet Green Tea Citrus bottles with a best by date of September 17, 2023.
We’ve drafted a message you can send PepsiCo to request your refund or repair — edit it as you like.
Subject: Recall F-1286-2023 — PepsiCo PepsiCo Hello, I own a PepsiCo that is covered by recall F-1286-2023 from PepsiCo. 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.
