(Bulk) Oyster, Frozen, Raw Half Shell, 15lb(6.8kg) UPC: 10087703078342 Harvest Dates: Jan 03,2025, Jan 14,2025
Summary
The FDA issued a Class II for (Bulk) Oyster, Frozen, Raw Half Shell, 15lb(6.8kg) UPC: 10087703078342 Harvest D by Wang Globalnet. Reason: Oyster product potentially contaminated with Norovirus.
Details
Source
Food Recall
External ID
H-0611-2025
Action Date
2025-09-24
Status
Terminated
Category
food
Product Description
(Bulk) Oyster, Frozen, Raw Half Shell, 15lb(6.8kg) UPC: 10087703078342 Harvest Dates: Jan 03,2025, Jan 14,2025
Lot/Code Info: Lot: B250103; B250114
Quantity Affected: 1,705 cases across both recalled lots
Reason for Recall
Oyster product potentially contaminated with Norovirus
Distribution
12 retail locations for lot# 250114 (Northeast states such as NJ, MA, NY) 15 retail locations for lot# 250103 (Southwest states such as CA, UT, CO)
Type: Voluntary: Firm initiated
Recall Initiated: 2025-08-07
Company
Vernon, 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 51 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (Wang Globalnet) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Wang Globalnet have FDA actions?
This is the only FDA action we have on record for Wang Globalnet in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0611-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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