CLASS I Food recall · Reported 3 Nov 2021 · FDA Enforcement Report

All products are stored refrigerated and labeled recalled

Kwokcheng Enterprise is recalling All products are stored refrigerated and labeled with Fullei Fresh Bean Sprouts in, distributed in Florida. The recall was initiated on 5 Oct 2021 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesAll Lots/Codes to include: 10 lb Bean Sprouts in box-Lots 251, 255, 258, 261, 264, 269, 268, 257, 252, 254, 259, 262, 265, 266 5 lb Bean Sprouts in box-Lots 251, 252, 254, 255, 257, 258, 259, 261, 262, 264, 265,266, 271, 8 oz Bean Sprout Pouches-Lots 251, 252, 254,258, 259, 261, 265, 263, 266, 268 4 oz Organic Bean Sprouts in clamshell-Lots 252, 254, 257, 259, 261, 264, 266, 268 5 lb Organic Bean Sprouts in box-Lots 257, 264, 271 10 lb SOY Sprouts (ALLERGEN)- Lots 252, 254, 257, 259, 261, 264, 266, 268 5 lb SOY Sprouts (ALLERGEN) Lots 254, 257, 261, 264, 268
Quantity recalled9438 pieces

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0068-2022
FDA event ID
88832
Recalling firm
Kwokcheng Enterprise, Miami, FL
Classification
Class I
Status
Terminated
Recall initiated
5 Oct 2021
FDA classified
22 Oct 2021
Reported
3 Nov 2021
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Listeria
Product category
Oysters & Shellfish

Timeline

5 Oct 2021Recall initiated by company
22 Oct 2021Classified by FDA+17 days
3 Nov 2021Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Firm is voluntarily recalling all lots/codes of bean and soy sprouts in commerce due to the potential for contamination with Listeria monocytogenes.

Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.

Product as listed by the FDA

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;

Where it was distributed

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.

Florida

Questions about this recall

Why was it recalled?

Firm is voluntarily recalling all lots/codes of bean and soy sprouts in commerce due to the potential for contamination with Listeria monocytogenes.

Which lots are affected?

All Lots/Codes to include: 10 lb Bean Sprouts in box-Lots 251, 255, 258, 261, 264, 269, 268, 257, 252, 254, 259, 262, 265, 266 5 lb Bean Sprouts in box-Lots 251, 252, 254, 255, 257, 258, 259, 261, 262, 264, 265,266, 271, 8 oz Bean Sprout Pouches-Lots 251, 252, 254,258, 259, 261, 265, 263, 266, 268 4 oz Organic Bean Sprouts in clamshell-Lots 252, 254, 257, 259, 261, 264, 266, 268 5 lb Organic Bean Sprouts in box-Lots 257, 264, 271 10 lb SOY Sprouts (ALLERGEN)- Lots 252, 254, 257, 259, 261, 264, 266, 268 5 lb SOY Sprouts (ALLERGEN) Lots 254, 257, 261, 264, 268

Where was it sold?

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.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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