Horizon Organic ORG ASEP CHOC MILK 1%
Reason Product has the potential to be spoiled.
Michel et Augustin brand Petites baguettes butter cookies Dark… recall
Recalled by Michel et Augustin Inc · Brooklyn, NY, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Undeclared hazelnuts due to miss-packaging by the foreign manufacturer.
Undeclared allergen: Tree nuts
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
Michel et Augustin brand Petites baguettes butter cookies Dark Chocolate with a pinch of salt, NET WT. 1.58 oz (45g), UPC 81266802016, Product of the Netherlands -- Manufactured for Michel et Augustin SA, 151 rue de Billancourt (Grand Paris) France --- The label states "May contain tree nuts and peanuts." but no nuts/tree nuts are listed in the ingredient statement.
Quantity: 2408 units (6-packs)
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.
Best Before 07 2016
Where it was sold
Connecticut New Jersey New York
FDA's distribution note: New York, New Jersey, Connecticut
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. The risk from an undeclared allergen is to people allergic to tree nuts; for anyone else the product is generally not a safety concern. 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
- Michel et Augustin Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Apr 7, 2016
- In FDA report of
- May 25, 2016
- Terminated
- May 20, 2016
- FDA recall number
- F-1365-2016 · event 73784
- Official record
- FDA enforcement report search
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