"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"
Class I - DangerousWhat Should You Do?
- Check if you have this product: All lots and codes. UPC 6921996166881
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Northern Food I/E Inc.
- Reason for Recall:
- Product contains undeclared sulfites (17.9mg/serving).
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full 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"
Product Codes/Lot Numbers:
All lots and codes. UPC 6921996166881
Distribution:
Distributed in: AL, CA, CT, FL, GA, IL, IN, LA, NY, NJ, OH, PA, TX
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: F-0212-2023
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