RecallHawk
Class I Recall

Nature's Wonder Premium Soybean Sprouts 12oz bag (UPC: 815098001347)

Chang & Son Enterprises, Inc.

Summary

The FDA issued a Class I for Nature's Wonder Premium Soybean Sprouts 12oz bag (UPC: 815098001347) by Chang & Son Enterprises, Inc.. Reason: Product may be contaminated with Listeria monocytogenes..

Details

Source

Food Recall

External ID

F-0964-2023

Action Date

2023-06-07

Status

Terminated

Category

food

Product Description

Nature's Wonder Premium Soybean Sprouts 12oz bag (UPC: 815098001347)

Lot/Code Info: All sell by dates before 5/28/2023. 12 oz bags - all product within expiry

Quantity Affected: 29,340 lbs

Reason for Recall

Product may be contaminated with Listeria monocytogenes.

Distribution

New York, Connecticut, Massachusetts, Rhode Island, Ohio, New Jersey, Maryland

Type: Voluntary: Firm initiated

Recall Initiated: 2023-05-05

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

Chang & Son Enterprises, Inc. has 3 FDA actions in our database, including 3 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 (Chang & Son Enterprises, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Chang & Son Enterprises, Inc. have FDA actions?

Chang & Son Enterprises, Inc. has 3 FDA actions in our database, including 3 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0964-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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