RecallHawk
Class II Recall

Post Honey Bunches of Oats with Almonds. Sweetened Cereal with Oats and Honey. Net Wt 48 oz (3 lbs) 1.36kg. 2 Bags ins

Post Consumer Brands, LLC

Summary

The FDA issued a Class II for Post Honey Bunches of Oats with Almonds. Sweetened Cereal with Oats and Honey. by Post Consumer Brands, LLC. Reason: Foreign Material (metal).

Details

Source

Food Recall

External ID

H-0044-2025

Action Date

2025-06-18

Status

Terminated

Category

food

Product Description

Post Honey Bunches of Oats with Almonds. Sweetened Cereal with Oats and Honey. Net Wt 48 oz (3 lbs) 1.36kg. 2 Bags inside for freshness. UPC 8 84912-01428 3. Post Consumer Brands, LLC, Lakeville, MN 55044.

Lot/Code Info: Best if Used By: APR0926 RCA, and APR1026 RCA

Quantity Affected: 5,376 units

Reason for Recall

Foreign Material (metal)

Distribution

CA, CO

Type: Voluntary: Firm initiated

Recall Initiated: 2025-05-28

Company

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

Post Consumer Brands, LLC has 2 FDA actions in our database, including 2 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 (Post Consumer Brands, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Post Consumer Brands, LLC have FDA actions?

Post Consumer Brands, LLC has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0044-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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