Matiz Piparra Peppers are packaged in a clear glass jar
Reason A shard of glass being found in one of the jars.
Blanxart 82% Congo Organic Chocolate Bar 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
A foreign object found by a consumer in a 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 82% Congo Organic Chocolate Bar. Paper packaging with internal foil wrapper. Net weight per bar: 4.4 oz. UPC 8 32924 00032 9. The product label is read in parts: "***BLANXART *** ORGANIC DARK CHOCOLATE 82% CONGO ***Ingredients: cocoa, cocoa butter, sugar, vanilla ***Imported By: Culinary Collective, Lynnwood, WA *** BB Chocolate Group, S.A C/Tambor del Bruc 13 17 08970 Sant Joan Desp¿ *** Made in Spain***".
Quantity: 24 cases (16 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.
BX 410, Lot 1931007 with date code stamp 30, Best by Date (BBD) of 8/2021. Product BX410 (importer code). 49054 (manufacturer code). Lot 1931007 with date code stamp 30.
Where it was sold
Illinois New York Vermont
FDA's distribution note: Distributed in IL, NY, VT and in Bermudas.
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
- Aug 27, 2020
- In FDA report of
- Sep 16, 2020
- Terminated
- Sep 18, 2020
- FDA recall number
- F-1425-2020 · event 86349
- Official record
- FDA enforcement report search
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