Hexing Haw Balls candy
Reason Unapproved dye Ponceau 4R
Koppers Chocolate Dark Chocolate Gummy Bears recall
Recalled by The Newark Nut Store · Linden, NJ, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Kopper s Chocolate has initiated recall of Koppers Chocolate Dark Chocolate Gummy Bears, 4oz (113g) retail package, metallized foil resealable pouch, 12 pouches per case, printed BB: 08/2020 because the product packaging only identifies soy as an allergen. The product does not list milk , which is an allergen .
Undeclared allergens: Milk Soy
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
Koppers Chocolate Dark Chocolate Gummy Bears, 4oz (113g) retail package, metallized foil resealable pouch, 12 pouches per case
Quantity: 25 cases (300 pouches) were distributed
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.
Lot code: 19001
Where it was sold
New Jersey New York Pennsylvania
FDA's distribution note: The product was distributed to NY, NJ, and PA retail locations
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, soy; 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
- The Newark Nut Store
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Sep 25, 2019
- In FDA report of
- Oct 30, 2019
- Terminated
- Jan 13, 2021
- FDA recall number
- F-0074-2020 · event 83961
- Official record
- FDA enforcement report search
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