Product is Frozen Half Shell Oysters in 15-16 pound blocks. Packaged in generic brown cardboard boxes. Side panel reads:
Summary
The FDA issued a Class II for Product is Frozen Half Shell Oysters in 15-16 pound blocks. Packaged in generic by Khee Trading, Inc.. Reason: Imported oysters potentially contaminated with Norovirus.
Details
Source
Food Recall
External ID
H-0482-2026
Action Date
2026-02-11
Status
Ongoing
Category
food
Product Description
Product is Frozen Half Shell Oysters in 15-16 pound blocks. 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 UPC: 850040844054
Lot/Code Info: Lot number: B250222 (Harvest Date: 2/22/2025) (Best By: 2/22/2027) B250310 (Harvest Date: 3/10/2025) (Best By: 3/10/2027) B250327 (Harvest Date: 3/27/2025) (Best By: 3/27/2027) B250330 (Harvest Date: 3/30/2025) (Best By: 3/30/2027) B250331 (Harvest Date: 3/31/2025) (Best By: 3/31/2027) B250226 (Harvest Date: 2/26/2025) (Best By: 2/26/2027) B250213 (Harvest Date: 2/13/2025) (Best By: 2/13/2027) B250416 (Harvest Date: 4/16/2025) (Best By: 4/16/2027) B250418 (Harvest Date: 4/18/2025) (Best By: 4/18/2027)
Quantity Affected: 7,306 cases across all recalled lots
Reason for Recall
Imported oysters potentially contaminated with Norovirus
Distribution
CA, NV, TX, CO, IL, ID, AZ
Type: Voluntary: Firm initiated
Recall Initiated: 2026-01-27
Company
Compton, CA
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 69 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-0482-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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