Feve Artisan Chocolatier x Dandelion Chocolate: Chocolate-covered cocoa nibs, 4 oz — FDA announcement Jun 25, 2024

Reported terminated

A company announcement posted by FDA. The listing date can differ from the original announcement date. The absence of a termination marker does not prove the recall is currently ongoing.

Source date Jun 25, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
Chocolate-covered cocoa nibs, 4 oz
Reason
Undeclared hazelnut allergen
Classification
Not supplied
Recalling firm
Feve Artisan Chocolatier and Dandelion Chocolate
Quantity
Not supplied
Agency-reported status
Terminated in FDA listing
Source record identifier
b3abd2c2762f9ed2

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Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicability6/24/2024, San Francisco, CA - Feve Artisan Chocolatier and Dandelion Chocolate are voluntarily recalling a single lot code of Feve Artisan Chocolatier x Dandelion Chocolate Chocolate-Covered Cocoa Nibs because the product may contain undeclared hazelnuts. People who have an allergy or severe sensitivity to hazelnuts run the risk of serious or life-threatening allergic reaction if they consume this product.; Batch Code: FNDHI4C4; Expiration Date: 3/14/2025; The recall was initiated after it was discovered that product containing hazelnuts was distributed in Chocolate-Covered Cocoa Nibs packaging that did not reveal the presence of this allergen. This issue was isolated to a single lot. No other lot codes, Feve Artisan Chocolatier, or Dandelion Chocolate products are included in this action. No illnesses have been reported.

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

Not supplied

No US distribution state could be established from this record. Check the official notice.

Dates in the source

Fda listing date
Jun 25, 2024
Company announcement date
Jun 24, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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