RecallHawk
Class II Recall

BREAKFAST BEST 12/13.4oz MXCS GRDL WFL PRTN 6BB 6BM-BKBST

Treehouse Foods

Summary

The FDA issued a Class II for BREAKFAST BEST 12/13.4oz MXCS GRDL WFL PRTN 6BB 6BM-BKBST by Treehouse Foods. Reason: potential to be contaminated with Listeria monocytogenes.

Details

Source

Food Recall

External ID

F-0151-2025

Action Date

2024-12-04

Status

Terminated

Category

food

Product Description

BREAKFAST BEST 12/13.4oz MXCS GRDL WFL PRTN 6BB 6BM-BKBST

Lot/Code Info: All Batch Codes starting with 2C and within shelf-life. Best By Dates: OCT 01 2024 to OCT 11 2025

Quantity Affected: 9,907,389 cases (total)

Reason for Recall

potential to be contaminated with Listeria monocytogenes

Distribution

Nationwide in USA and Canada

Type: Voluntary: Firm initiated

Recall Initiated: 2024-10-17

Company

Treehouse Foods

Oak Brook, IL

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 82 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Treehouse Foods has 69 FDA actions in our database, including 69 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 (Treehouse Foods) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Treehouse Foods have FDA actions?

Treehouse Foods has 69 FDA actions in our database, including 69 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0151-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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