Fruit Juice Candy Bonbons de Jus de Fruits
Reason The Florida Dept of Agriculture sample tested positive for lead at concentration of 0.226 ppm (ug/g).
Meiqili Durian Candy in plastic bag with clear window recall
Recalled by Fine Land Corp · 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
Meiqili Durian Candy in plastic bag with clear window, Net Wt: 12 ounce (340 g). It is a labeled as a product of P.R.C. and has a UPC code of 4-897055-795465-0. Sole Agent of U.S.A.: Fine Land Corp.
Quantity: 51
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.
N/A
Where it was sold
Connecticut Massachusetts Maryland New York Virginia
FDA's distribution note: Connecticut, New York, Philadelphia, Virginia, Maryland and Massachusetts
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
- Fine Land Corp
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Oct 10, 2018
- In FDA report of
- Feb 6, 2019
- Terminated
- Feb 5, 2019
- FDA recall number
- F-0794-2019 · event 81733
- Official record
- FDA enforcement report search
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