RecallHawk
Class III Recall

Lipton Diet Green Tea Citrus, 24 pack of 16.9floz bottles. UPC # 0-12000-01722-3

Pepsico Inc

Summary

The FDA issued a Class III for Lipton Diet Green Tea Citrus, 24 pack of 16.9floz bottles. UPC # 0-12000-01722- by Pepsico Inc. Reason: Undeclared aspartame and lack of Phenylketonurics warning on immediate container (16.9fl.oz. bottle).

Details

Source

Food Recall

External ID

F-1286-2023

Action Date

2023-07-26

Status

Terminated

Category

food

Product Description

Lipton Diet Green Tea Citrus, 24 pack of 16.9floz bottles. UPC # 0-12000-01722-3

Lot/Code Info: SEP172023XXXXAG06133 Best by Date SEP 17 2023

Quantity Affected: 300, 24 packs (retail unit)

Reason for Recall

Undeclared aspartame and lack of Phenylketonurics warning on immediate container (16.9fl.oz. bottle)

Distribution

IN, TN, OH, KY

Type: Voluntary: Firm initiated

Recall Initiated: 2023-07-08

Company

Pepsico Inc

Purchase, NY

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 61 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 III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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-1286-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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