Hexing Haw Balls candy
Reason Unapproved dye Ponceau 4R
Jacques Big Daddy Dark Chocolate Bar recall
Recalled by Jacques Torres Manufacturing , llc. · Brooklyn, NY, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Product contains undeclared milk.
Undeclared allergen: Milk
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
Jacques Big Daddy Dark Chocolate Bar. The product comes in un-coded 2.2 lbs. (1kg) clear plastic package overwrapped with reddish brown paper label.
Quantity: 293 bars
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.
Not Coded
Where it was sold
California Colorado Connecticut Florida Georgia Massachusetts Maryland Minnesota New Jersey New Mexico New York South Carolina Texas Virginia Vermont Washington Wisconsin
FDA's distribution note: California, Connecticut, New York, Maryland, Florida, south Carolina, Massachusetts, New Mexico, Vermont, Texas, Virginia, New Jersey, Washington, Wisconsin, Minnesota, Colorado, Georgia, Through Jacques Torres Chocolate retail stores and mrchocolate.com (e commerce of Jacques Torres Manufacturing)
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 milk; 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
- Jacques Torres Manufacturing , llc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Feb 4, 2019
- In FDA report of
- Apr 3, 2019
- Terminated
- Aug 21, 2019
- FDA recall number
- F-1187-2019 · event 82208
- Official record
- FDA enforcement report search
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