Recall record at a glance
| Official record | F-0068-2022 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Kwokcheng Enterprise, Inc. dba Fullei Fresh |
| Report date | Nov 3, 2021 |
| Recall initiation date | Oct 5, 2021 |
| Quantity | 9438 pieces |
| Location | Miami, FL, United States |
Official product description
All products are stored refrigerated and labeled with Fullei Fresh brand. 10 lb Bean Sprouts in cardboard box; 5 lb Bean Sprouts in cardboard box; 8 bags of 8 oz Bean Sprout Pouches (Pouched then placed in cardboard box); 8 bags of 4 oz Organic Bean Sprouts (in plastic clamshell then in cardboard box); 5 lb Organic Bean Sprouts in cardboard box; 10 lb SOY Sprouts (ALLERGEN) in cardboard box; 5 lb SOY Sprouts (ALLERGEN) in cardboard box;
Why the product was recalled
Firm is voluntarily recalling all lots/codes of bean and soy sprouts in commerce due to the potential for contamination with Listeria monocytogenes.
Distribution information
All bean and soy sprout consignees are within the state of Florida. The firm owns refrigerated delivery trucks that transport the sprouts to the customers directly. No third party delivery service is used.
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.