RecallHawk
Class I Recall

365 Whole Foods Market Small Bites Macaroni & Cheese. Net Wt 8.5 oz (240g) Keep Frozen. UPC 99482499709. Distributed

C.H. Guenther & Son LLC

Summary

The FDA issued a Class I for 365 Whole Foods Market Small Bites Macaroni & Cheese. Net Wt 8.5 oz (240g) Kee by C.H. Guenther & Son LLC. Reason: Undeclared allergen (eggs) and pork.

Details

Source

Food Recall

External ID

F-0702-2025

Action Date

2025-04-16

Status

Terminated

Category

food

Product Description

365 Whole Foods Market Small Bites Macaroni & Cheese. Net Wt 8.5 oz (240g) Keep Frozen. UPC 99482499709. Distributed by: Whole Foods Market, Austin, TX

Lot/Code Info: Best-By Date: 11/29/25

Quantity Affected: 1818 cases

Reason for Recall

Undeclared allergen (eggs) and pork

Distribution

Nationwide

Type: Voluntary: Firm initiated

Recall Initiated: 2025-03-11

Company

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 32 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

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 (C.H. Guenther & Son LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does C.H. Guenther & Son LLC have FDA actions?

This is the only FDA action we have on record for C.H. Guenther & Son LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0702-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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