RecallHawk
Class I Recall

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

Santa Monica Seafood Company

Summary

The FDA issued a Class I for Atlantic Salmon Portions with Seafood Stuffing; 16 OZ (1 LB) 454g; Use/Freeze By by Santa Monica Seafood Company. Reason: Atlantic Salmon Portions with Seafood Stuffing was incorrectly labeled and does not declare allergen ingredient (SOY).

Details

Source

Food Recall

External ID

H-0043-2025

Action Date

2025-06-18

Status

Terminated

Category

food

Product Description

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

Lot/Code Info: Lot#: 197940521

Quantity Affected: 150 cases

Reason for Recall

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

Distribution

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

Type: Voluntary: Firm initiated

Recall Initiated: 2025-05-24

Company

Santa Monica Seafood Company

Rancho Dominguez, CA

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 161 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

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 (Santa Monica Seafood Company) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Santa Monica Seafood Company have FDA actions?

This is the only FDA action we have on record for Santa Monica Seafood Company in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0043-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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