FDA recall record

Pepsico Lipton Iced Tea Peach, 24 Pack retail unit, 24 - 16.9 FL OZ recall — FDA F-0982-2022

Immediate package (individual 16.9 FL OZ bottle) is incorrectly labeled as the zero sugar variety, the product inside the bottle is the sugar containing…

Class IIclassification
F-0982-2022official record ID
Apr 20, 2022report date

Recall record at a glance

Official recordF-0982-2022
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmPepsico Inc.
Report dateApr 20, 2022
Recall initiation dateApr 2, 2022
Quantity780 - 24 pack cases
LocationPurchase, NY, United States

Official product description

Lipton Iced Tea Peach, 24 Pack retail unit, 24 - 16.9 FL OZ Bottles. UPC on retail 24 pack: 012000023118

Why the product was recalled

Immediate package (individual 16.9 FL OZ bottle) is incorrectly labeled as the zero sugar variety, the product inside the bottle is the sugar containing variety

Distribution information

IN, TN, OH, KY

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.