Recall Radar

Disclaimer: Recall Radar is an informational summary of public FDA enforcement reports. It is not medical advice. Always confirm details with the FDA, the company, a pharmacist, or a doctor before making health decisions.

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Class IFood

Fromagerie Coop de Mean Cabricharme and Belgium… recall

Summary

WFM Purchasing, LP is recalling Fromagerie Coop de Mean Cabricharme and Belgium Cabricharme Shelf life (food). According to the FDA report, the reason is: Undeclared Egg Allergen. The FDA rated this a Class I: most serious: there is a reasonable chance the product could cause serious health problems or death. Recall status: Ongoing.

Understanding this recall

What happened

Whole Foods Market's purchasing arm (WFM Purchasing) is recalling Cabricharme cheese because it contains egg that isn't declared on the label.

Why it matters

Egg is one of the major food allergens and is especially common in young children. Undeclared egg can cause allergic reactions, including severe ones, in people who rely on labels to avoid it.

Who should pay attention

People with egg allergies who bought this cheese at Whole Foods in CA, AZ, NJ, MA, RI, CT or NY.
Distribution in the FDA report: CA, AZ, NJ, MA, RI, CT, NY

How to check your product

The report covers all dates through and including 10/7/2026. Check the date on the cheese wrapping or store label.
Codes listed by the FDA: Shelf life: 30 days, all dates through and including 10/7/2026

Based only on the FDA enforcement record plus general public-health background on this type of hazard. Not medical advice; if you have symptoms or concerns, contact a doctor or pharmacist.

Details from the FDA report

Product
Fromagerie Coop de Mean Cabricharme and Belgium Cabricharme Shelf life: 30 days, all dates through and including 10/7/2026 Packaging: Plastic wrapped by slice Net Wt.: Various, cut from whole wheel and priced by weight with Whole Foods Market scale label PLUs: 54670, 57953
Reason
Undeclared Egg Allergen
Lot / code info
Shelf life: 30 days, all dates through and including 10/7/2026
Quantity
21 Wheels
Distribution
CA, AZ, NJ, MA, RI, CT, NY
Recalling company
WFM Purchasing, LP, Austin, TX United States
Recall started
September 8, 2026
FDA report date
September 30, 2026
Classification
Class I: Most serious: there is a reasonable chance the product could cause serious health problems or death.
Voluntary / mandated
Voluntary: Firm initiated
Status
Ongoing
Recall number
H-1395-2026

What to do

View the FDA source record (openFDA) · FDA recalls page

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