WFM Purchasing, LP food recall: Fromagerie Coop de Mean Cabricharme and Belgium Cabricharme Shelf…
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Ongoing
- Event ID
- 99874
- Recall initiated
- Sep 8, 2026
- Classified by FDA
- Sep 22, 2026
- Posted in Enforcement Report
- Sep 30, 2026
- Recalling firm
- WFM Purchasing, LP
- Firm location
- Austin, TX, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Products in this event
- 1
What to do
Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.
Reason for recall
Undeclared Egg Allergen
What the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on Sep 8, 2026. FDA classified it 14 days later, on Sep 22, 2026. Distribution reported by FDA: CA, AZ, NJ, MA, RI, CT, NY WFM Purchasing, LP has 5 recalls in our records.
Recalled products (1)
H-1395-2026 Class I Ongoing
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
Codes / lots: Shelf life: 30 days, all dates through and including 10/7/2026
Quantity: 21 Wheels
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
- Official notice
- FDA Enforcement Report, event 99874
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.