RecallHawk
Class II Recall

Product is Frozen Half Shell Oysters in 15 pound blacks. Packaged in generic brown cardboard boxes. Side panel reads: H

Khee Trading, Inc.

Summary

The FDA issued a Class II for Product is Frozen Half Shell Oysters in 15 pound blacks. Packaged in generic bro by Khee Trading, Inc.. Reason: Imported Frozen Oyster potentially contaminated with Norovirus..

Details

Source

Food Recall

External ID

H-0521-2025

Action Date

2025-08-27

Status

Ongoing

Category

food

Product Description

Product is Frozen Half Shell Oysters in 15 pound blacks. Packaged in generic brown cardboard boxes. Side panel reads: HAFL SHELL OYSTER Spec: 144PCS; Imported by: Khee Trading Inc., Compton, CA Side panel reads: Method of harvest: Farm Raised Country of Origin: Republic of Korea ICSSL NO: KR-15-SP No UPC

Lot/Code Info: B250112

Quantity Affected: 98 cartons

Reason for Recall

Imported Frozen Oyster potentially contaminated with Norovirus.

Distribution

Distribution is 8 distributor consignees across California, NV, AZ and TX.

Type: Voluntary: Firm initiated

Recall Initiated: 2025-08-05

Company

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 90 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Khee Trading, Inc. has 3 FDA actions in our database, including 3 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

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 (Khee Trading, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Khee Trading, Inc. have FDA actions?

Khee Trading, 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 "H-0521-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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