CLASS I ONGOING Food recall · Reported 30 Sep 2026 · FDA Enforcement Report
Fromagerie Coop de Mean Cabricharme recalled by WFM Purchasing
WFM Purchasing is recalling Fromagerie Coop de Mean Cabricharme and Belgium Cabricharme Shelf life: 30 days, all, distributed in 7 states. The recall was initiated on 8 Sep 2026 and the FDA has classified it as Class I.
Check your package
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-1395-2026
- FDA event ID
- 99874
- Recalling firm
- WFM Purchasing, Austin, TX
- Brand
- Fromagerie Coop
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 8 Sep 2026
- FDA classified
- 22 Sep 2026
- Reported
- 30 Sep 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Undeclared Egg
- Product category
- Other
Timeline
| 8 Sep 2026 | Recall initiated by company | |
| 22 Sep 2026 | Classified by FDA | +14 days |
| 30 Sep 2026 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Undeclared Egg Allergen
Product as listed by the FDA
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
Where it was distributed
CA, AZ, NJ, MA, RI, CT, NY
ArizonaCaliforniaConnecticutMassachusettsNew JerseyNew YorkRhode Island
Stores named: Whole Foods
Questions about this recall
Why was it recalled?
Undeclared Egg Allergen
Which lots are affected?
Shelf life: 30 days, all dates through and including 10/7/2026
Where was it sold?
CA, AZ, NJ, MA, RI, CT, NY
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 6 Oct 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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