RecallHawk
Class I Recall

Fullei Fresh brand Alfalfa Sprouts in a 4 oz. clear plastic clamshell container; UPC Code 17442 30012. Packaged in 5lb c

Kwokcheng Enterprise, Inc. dba Fullei Fresh

Summary

The FDA issued a Class I for Fullei Fresh brand Alfalfa Sprouts in a 4 oz. clear plastic clamshell container; by Kwokcheng Enterprise, Inc. dba Fullei Fresh. Reason: Possible contamination with Shiga toxin-producing E. coli (non-O157:H7 STEC).

Details

Source

Food Recall

External ID

F-0324-2023

Action Date

2023-02-08

Status

Terminated

Category

food

Product Description

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

Lot/Code Info: Lot:336; Sell by: Jan 06 2023

Quantity Affected: Total of 333 cases consisting of 20 cases of 5lb, 30 cases of 12pk, 283 cases of 8pk

Reason for Recall

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

Distribution

FL

Type: Voluntary: Firm initiated

Recall Initiated: 2022-12-28

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 32 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Kwokcheng Enterprise, Inc. dba Fullei Fresh 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 (Kwokcheng Enterprise, Inc. dba Fullei Fresh) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Kwokcheng Enterprise, Inc. dba Fullei Fresh have FDA actions?

Kwokcheng Enterprise, Inc. dba Fullei Fresh 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-0324-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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