RecallHawk
Class III Recall

12 oz Aluminum cans of root beer packaged 12 cans per carton. 2/12pks per case

Pepsico Inc.

Summary

The FDA issued a Class III for 12 oz Aluminum cans of root beer packaged 12 cans per carton. 2/12pks per case by Pepsico Inc.. Reason: Product was mislabeled. Can labeled as regular Mug contains Mug Zero Sugar.

Details

Source

Food Recall

External ID

F-1203-2024

Action Date

2024-05-01

Status

Terminated

Category

food

Product Description

12 oz Aluminum cans of root beer packaged 12 cans per carton. 2/12pks per case

Lot/Code Info: JUL2224XXXXAS02234, Best by Date JUL 22 2024

Quantity Affected: 2,801 - 12 pack cases

Reason for Recall

Product was mislabeled. Can labeled as regular Mug contains Mug Zero Sugar

Distribution

AR, TX, LA, MS, NM, OK

Type: Voluntary: Firm initiated

Recall Initiated: 2024-03-22

Company

Pepsico Inc.

Valhalla, 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 32 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-1203-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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