Food Recall Check
Class II · Moderate risk Terminated Initiated Mar 17, 2021 (6 years ago)

Blanxart Milk Chocolate with Hazelnuts Cacao 33% Min recall

Recalled by Power Selles Imports dba Culinary Collective · Lynnwood, WA, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Metal fragment. The small thin metal piece is around 0.5 inch long without sharp edges, was found inside chocolate bar.

Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.

What was recalled

Blanxart Milk Chocolate with Hazelnuts Cacao 33% Min. Net wt.7 oz. Product is packaged with paper and internal foil wrapper. UPC 6 66785 20322 9. The label is read in parts: "***BLANXART Milk Chocolate with Hazelnuts CACAO 33% *** BB Chocolate Grup, S.A Tambor del Bruc 13 08970 Sant Joan Despi Barcelona, Spain *** Imported By: Culinary Collective Lynnwood, WA ***".

Quantity: 12 cases (11/7 oz. bars per case)

Food: Chocolate & candy

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Code BX203, Case lot # 2047026, Unit lot # Lot 81030, best by date of 01/2022.

Where it was sold

Massachusetts New York Oregon Washington

FDA's distribution note: distributed in MA, NY, OR, and WA.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Power Selles Imports dba Culinary Collective
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 17, 2021
In FDA report of
Apr 7, 2021
Terminated
Apr 27, 2021
FDA recall number
F-0365-2021 · event 87544
Official record
FDA enforcement report search

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