CLASS III Food recall · Reported 1 May 2024 · FDA Enforcement Report

Aluminum cans of root beer packaged recalled by Pepsico

Pepsico is recalling Aluminum cans of root beer packaged per, distributed in Arkansas, Louisiana, Mississippi, New Mexico, Oklahoma, Texas. The recall was initiated on 22 Mar 2024 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesJUL2224XXXXAS02234, Best by Date JUL 22 2024
Quantity recalled2,801 - 12 pack cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1203-2024
FDA event ID
94357
Recalling firm
Pepsico, Valhalla, NY
Classification
Class III
Status
Terminated
Recall initiated
22 Mar 2024
FDA classified
24 Apr 2024
Reported
1 May 2024
Type
Voluntary: Firm initiated
Customers notified by
Visit
Reason category
Labeling Errors
Product category
Soda

Timeline

22 Mar 2024Recall initiated by company
24 Apr 2024Classified by FDA+33 days
1 May 2024Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Product as listed by the FDA

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

Where it was distributed

AR, TX, LA, MS, NM, OK

ArkansasLouisianaMississippiNew MexicoOklahomaTexas

Questions about this recall

Why was it recalled?

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

Which lots are affected?

JUL2224XXXXAS02234, Best by Date JUL 22 2024

Where was it sold?

AR, TX, LA, MS, NM, OK

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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