RecallHawk
Class II Recall

Lipton Green Tea Citrus. 16.9 ounce PET Bottle. sold as 12pk. Outer case label reads as , "*** Lipton Green Tea Citrus (

Pepsico Inc

Summary

The FDA issued a Class II for Lipton Green Tea Citrus. 16.9 ounce PET Bottle. sold as 12pk. Outer case label r by Pepsico Inc. Reason: Undeclared sugar in finished product-primary package does not reflect the product inside bottle..

Details

Source

Food Recall

External ID

H-0010-2026

Action Date

2025-10-08

Status

Terminated

Category

food

Product Description

Lipton Green Tea Citrus. 16.9 ounce PET Bottle. sold as 12pk. Outer case label reads as , "*** Lipton Green Tea Citrus (25g sugar)***" Individual bottle label reads as "*** Lipton Diet Green Tea Mixed Berry (0g sugar)***). Shelf stable.

Lot/Code Info: Individual bottles and 12 pack outer wrap: DEC 01 25. HHMM DW 08035

Quantity Affected: 2,854 Cases, 2-12 pack units equal a case

Reason for Recall

Undeclared sugar in finished product-primary package does not reflect the product inside bottle.

Distribution

Products distributed in the following states: AZ, CO, NM, UT, TX, KS, NE, OK, WY, and SD.

Type: Voluntary: Firm initiated

Recall Initiated: 2025-09-17

Company

Pepsico Inc

Purchase, NY

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 39 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Pepsico Inc has 11 FDA actions in our database, including 11 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Pepsico Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Pepsico Inc have FDA actions?

Pepsico Inc has 11 FDA actions in our database, including 11 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0010-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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