CLASS I Food recall · Reported 8 Feb 2023 · FDA Enforcement Report

Fullei Fresh Alfalfa Sprouts in a container recalled

Kwokcheng Enterprise is recalling Fullei Fresh Alfalfa Sprouts in a container, distributed in Florida. The recall was initiated on 28 Dec 2022 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot:336; Sell by: Jan 06 2023
Quantity recalledTotal of 333 cases consisting of 20 cases of 5lb, 30 cases of 12pk, 283 cases of 8pk

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-0324-2023
FDA event ID
91439
Recalling firm
Kwokcheng Enterprise, Miami, FL
Brand
Fullei
Classification
Class I
Status
Terminated
Recall initiated
28 Dec 2022
FDA classified
31 Jan 2023
Reported
8 Feb 2023
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
E. coli
Product category
Oysters & Shellfish

Timeline

28 Dec 2022Recall initiated by company
31 Jan 2023Classified by FDA+34 days
8 Feb 2023Published in enforcement report+8 days

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

Reason for recall

Possible contamination with Shiga toxin-producing E. coli (non-O157:H7 STEC)

Some strains of E. coli, such as O157:H7, produce a toxin that can cause severe stomach cramps, bloody diarrhea and, in a small number of cases, kidney failure.

Product as listed by the FDA

Fullei Fresh brand Alfalfa Sprouts in a 4 oz. clear plastic clamshell container; UPC Code 17442 30012. Packaged in 5lb carboard box 12 packages of 4 oz

Where it was distributed

FL

Florida

Questions about this recall

Why was it recalled?

Possible contamination with Shiga toxin-producing E. coli (non-O157:H7 STEC)

Which lots are affected?

Lot:336; Sell by: Jan 06 2023

Where was it sold?

FL

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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