Mut Dua Non YOUNG COCONUT CANDY
Reason The product was found to contain undeclared sulfites (258.6 ppm) plus undeclared colors Yellow #5, Blue #1 and Red #3 based on sampling and analysis by New York State Department of Agriculture & Markets.
VINA CAF¿ WAKE-UP INSTANT COFFEE MIX in recall
Recalled by Hong Lee Trading · Brooklyn, NY, United States
Class I — High risk. Reasonable probability of serious harm or death.
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
VINA CAF¿ WAKE-UP INSTANT COFFEE MIX in 18 PACK CARDBOARD BOXES (.6 oz packs); UPC: 8 934683 002759
Quantity: 70 cartons
Food: Juice & beverages
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.
EXP:17.MAR.2019 1T13
Where it was sold
Connecticut New Jersey New York
FDA's distribution note: Importer sold product to: NY, NJ, CT
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. 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
- Hong Lee Trading
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Sep 28, 2017
- In FDA report of
- Oct 25, 2017
- Terminated
- Jul 19, 2018
- FDA recall number
- F-0026-2018 · event 78230
- Official record
- FDA enforcement report search
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