Beijing Hawthorne Candy
Reason Product contains undeclared sulfites (7.32 mg/serving)
Lukai sweetened jujube" recall
Recalled by Northern Food I/E Inc. · Westbury, NY, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Product contains undeclared sulfites (17.9mg/serving).
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
"Lukai sweetened jujube"; 8.3 ounces; red and yellow packaging; back panel states: "Name: Ejiao dates; Ingredients: a nuclear-free golden jujube, donkey-hide gelatin, sugar, honey, maltose, citric acid; Consumption methods: open bags of ready-to-eat, soup, making cakes; Shelf life: 12 months; Place of Origin: China Chengdu; Storage: Please store in a dry well-ventilated place, or frozen better; American General Agency: NORTHERN FOOD I/E INC"
Quantity: 41 cartons
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.
All lots and codes. UPC 6921996166881
Where it was sold
Alabama California Connecticut Florida Georgia Illinois Indiana Louisiana New Jersey New York Ohio Pennsylvania Texas
FDA's distribution note: AL, CA, CT, FL, GA, IL, IN, LA, NY, NJ, OH, PA, TX
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. 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
- Northern Food I/E Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Dec 5, 2022
- In FDA report of
- Jan 4, 2023
- Terminated
- Apr 21, 2023
- FDA recall number
- F-0212-2023 · event 91285
- Official record
- FDA enforcement report search