Food Recall Check
Class I · High risk Terminated Initiated May 24, 2025 (17 months ago)

Atlantic Salmon Portions with Seafood Stuffing recall

Recalled by Santa Monica Seafood Company · Rancho Dominguez, CA, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Atlantic Salmon Portions with Seafood Stuffing was incorrectly labeled and does not declare allergen ingredient (SOY)

Undeclared allergens: Soy Fish

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

Atlantic Salmon Portions with Seafood Stuffing; 16 OZ (1 LB) 454g; Use/Freeze By: JUN.02.25; UPC: 4061459716313

Quantity: 150 cases

Food: Seafood & fish

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot#: 197940521

Where it was sold

FDA's distribution note: Product is a private label exclusively for Aldi Inc. Firm is still collecting distribution information and number of retail locations that received product.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to soy, fish; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Santa Monica Seafood Company
Initiated by
Voluntary: Firm initiated
Recall initiated
May 24, 2025
In FDA report of
Jun 18, 2025
Terminated
Jun 26, 2025
FDA recall number
H-0043-2025 · event 96951
Official record
FDA enforcement report search

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