CLASS I Food recall · Reported 17 Dec 2025 · FDA Enforcement Report

Charlevoix Cheese Company Mild Cheddar Cheese recalled

Boss Dairy Farms is recalling Charlevoix Cheese Company Mild Cheddar Cheese, distributed in Michigan. The recall was initiated on 16 Nov 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot 13220025
Quantity recalled420 units

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
H-0248-2026
FDA event ID
98041
Recalling firm
Boss Dairy Farms, Charlevoix, MI
Classification
Class I
Status
Terminated
Recall initiated
16 Nov 2025
FDA classified
10 Dec 2025
Reported
17 Dec 2025
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Listeria
Product category
Cheese

Timeline

16 Nov 2025Recall initiated by company
10 Dec 2025Classified by FDA+24 days
17 Dec 2025Published 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

Possible Listeria monocytogenes contamination.

Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.

Product as listed by the FDA

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

Where it was distributed

MI

Michigan

Questions about this recall

Why was it recalled?

Possible Listeria monocytogenes contamination.

Which lots are affected?

Lot 13220025

Where was it sold?

MI

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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

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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