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