RecallHawk
Class I Recall

Charlevoix Cheese Company Mild Cheddar Cheese, Net Wt. 8 oz (227g). UPC 8 50056-64205 7. 12 retail units per wholesale

Boss Dairy Farms

Summary

The FDA issued a Class I for Charlevoix Cheese Company Mild Cheddar Cheese, Net Wt. 8 oz (227g). UPC 8 50056 by Boss Dairy Farms. Reason: Possible Listeria monocytogenes contamination..

Details

Source

Food Recall

External ID

H-0248-2026

Action Date

2025-12-17

Status

Terminated

Category

food

Product Description

Charlevoix Cheese Company Mild Cheddar Cheese, Net Wt. 8 oz (227g). UPC 8 50056-64205 7. 12 retail units per wholesale case.

Lot/Code Info: Lot 13220025

Quantity Affected: 420 units

Reason for Recall

Possible Listeria monocytogenes contamination.

Distribution

MI

Type: Voluntary: Firm initiated

Recall Initiated: 2025-11-16

Company

Boss Dairy Farms

Charlevoix, MI

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 105 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 (Boss Dairy Farms) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Boss Dairy Farms have FDA actions?

This is the only FDA action we have on record for Boss Dairy Farms in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0248-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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