Frozen Oyster Meat (IQF), Cert No. KR-15-SP; Processor Name: JBR KR-15-SP; Harvest Date: Feb 06, 2025 Shucked Date: Feb
Summary
The FDA issued a Class II for Frozen Oyster Meat (IQF), Cert No. KR-15-SP; Processor Name: JBR KR-15-SP; Harv by Jayone Foods, Inc.. Reason: Frozen Oyster product is potentially contaminated with Norovirus.
Details
Source
Food Recall
External ID
H-0500-2025
Action Date
2025-08-20
Status
Terminated
Category
food
Product Description
Frozen Oyster Meat (IQF), Cert No. KR-15-SP; Processor Name: JBR KR-15-SP; Harvest Date: Feb 06, 2025 Shucked Date: Feb 07,2025 Expiration: 02/06/2027 UPC: 8809366955717
Lot/Code Info: Lot Code: B250206
Quantity Affected: 225 cartons
Reason for Recall
Frozen Oyster product is potentially contaminated with Norovirus
Distribution
Distribution is limited to 1 wholesale distributor and 3 supermarket locations in Southern California.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-07-31
Company
Paramount, 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 113 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Jayone Foods, Inc. has 2 FDA actions in our database, including 2 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 (Jayone Foods, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Jayone Foods, Inc. have FDA actions?
Jayone Foods, Inc. 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 "H-0500-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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