"Lukai sweetened jujube"; 8.3 ounces; red and yellow packaging; back panel states: "Name: Ejiao dates; Ingredients: a nu
Summary
The FDA issued a Class I for "Lukai sweetened jujube"; 8.3 ounces; red and yellow packaging; back panel state by Northern Food I/E Inc.. Reason: Product contains undeclared sulfites (17.9mg/serving)..
Details
Source
Food Recall
External ID
F-0212-2023
Action Date
2023-01-04
Status
Terminated
Category
food
Product Description
"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"
Lot/Code Info: All lots and codes. UPC 6921996166881
Quantity Affected: 41 cartons
Reason for Recall
Product contains undeclared sulfites (17.9mg/serving).
Distribution
AL, CA, CT, FL, GA, IL, IN, LA, NY, NJ, OH, PA, TX
Type: Voluntary: Firm initiated
Recall Initiated: 2022-12-05
Company
Westbury, NY
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 18 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Northern Food I/E Inc. has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Northern Food I/E Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Northern Food I/E Inc. have FDA actions?
Northern Food I/E Inc. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0212-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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