Hexing Haw Balls candy
Reason Unapproved dye Ponceau 4R
GANCHI NAIWEITANGPIAN Candy recall
Recalled by Rong Shing Trading Inc. · 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
GANCHI NAIWEITANGPIAN Candy NET WT: 280G(9.8oz) in cardboard package. 24 packages per master case. The following codes are listed on the individual packages: 20190316 (stamped on box), BEST BEFORE: 03.15.2020, UPC 6926106100083. INGREDIENTS: sugar, glucose, planting the fat end, (glucose syrup, soybean oil, shortening, casein acid sodium, span 60, FD&C Yellow 5). RONG SHING TRADING NY INC. 47-57 BRIDGEWATER STREET BROOKLYN NY 11222.
Quantity: 54 cartons; 24 packages/carton; Total: 1,296 packages
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.
20190316 (stamped on box), BEST BEFORE: 03.15.2020, UPC 6926106100083
Where it was sold
Kentucky Maryland New York Utah Virginia Vermont Washington
FDA's distribution note: Retailer in 7 states: KY, MD, NY, UT, VA, VT, 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. 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
- Rong Shing Trading Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Sep 26, 2019
- In FDA report of
- Nov 6, 2019
- Terminated
- Mar 31, 2021
- FDA recall number
- F-0091-2020 · event 83898
- Official record
- FDA enforcement report search
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