Fresh Chilean Salmon Fillet, Net WT (variable weight) 50 lb brown corrugated carboard box (up to 6 fillets per box). Box
Summary
The FDA issued a Class II for Fresh Chilean Salmon Fillet, Net WT (variable weight) 50 lb brown corrugated car by Moon N Sea GA LLC. Reason: RTE fish (sushi-salmon, tuna) processed under insanitary conditions. The firm was notified by the Georgia Department of Agriculture that the products .
Details
Source
Food Recall
External ID
H-0350-2025
Action Date
2025-08-06
Status
Terminated
Category
food
Product Description
Fresh Chilean Salmon Fillet, Net WT (variable weight) 50 lb brown corrugated carboard box (up to 6 fillets per box). Boxes contain ice for temperature control. Keep Refrigerated.
Lot/Code Info: No printed expiration dates all products were delivered fresh within 1~2 days of processing
Quantity Affected: 1051.14 lb
Reason for Recall
RTE fish (sushi-salmon, tuna) processed under insanitary conditions. The firm was notified by the Georgia Department of Agriculture that the products were manufactured under unsanitary conditions.
Distribution
Products were shipped to the following states: Alabama (AL), Georgia (GA), South Carolina (SC) & Tennessee (TN). All products were sold in bulk. No press release was requested from the firm.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-06-24
Company
Buford, GA
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 85 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Moon N Sea GA LLC has 4 FDA actions in our database, including 4 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 (Moon N Sea GA LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Moon N Sea GA LLC have FDA actions?
Moon N Sea GA LLC has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0350-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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