Lipton Iced Tea Peach, 24 Pack retail unit, 24 - 16.9 FL OZ Bottles. UPC on retail 24 pack: 012000023118
Summary
The FDA issued a Class II for Lipton Iced Tea Peach, 24 Pack retail unit, 24 - 16.9 FL OZ Bottles. UPC on ret by Pepsico Inc. Reason: Immediate package (individual 16.9 FL OZ bottle) is incorrectly labeled as the zero sugar variety, the product inside the bottle is the sugar containi.
Details
Source
Food Recall
External ID
F-0982-2022
Action Date
2022-04-20
Status
Terminated
Category
food
Product Description
Lipton Iced Tea Peach, 24 Pack retail unit, 24 - 16.9 FL OZ Bottles. UPC on retail 24 pack: 012000023118
Lot/Code Info: JUL2422XXXXAG03252 Best By Date JUL 24 22
Quantity Affected: 780 - 24 pack cases
Reason for Recall
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
IN, TN, OH, KY
Type: Voluntary: Firm initiated
Recall Initiated: 2022-04-02
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 40 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 "F-0982-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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