Santa Monica Seafood Company food recall: Atlantic Salmon Portions with Seafood Stuffing
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Terminated
- Event ID
- 96951
- Recall initiated
- May 24, 2025
- Classified by FDA
- Jun 12, 2025
- Posted in Enforcement Report
- Jun 18, 2025
- Terminated
- Jun 26, 2025
- Recalling firm
- Santa Monica Seafood Company
- Firm location
- Rancho Dominguez, CA, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Press Release
- Products in this event
- 1
What to do
Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.
Reason for recall
Atlantic Salmon Portions with Seafood Stuffing was incorrectly labeled and does not declare allergen ingredient (SOY)
What the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on May 24, 2025. FDA classified it 19 days later, on Jun 12, 2025. Distribution reported by FDA: Product is a private label exclusively for Aldi Inc. Firm is still collecting distribution information and number of retail locations that received product.
Recalled products (1)
H-0043-2025 Class I Terminated
Atlantic Salmon Portions with Seafood Stuffing; 16 OZ (1 LB) 454g; Use/Freeze By: JUN.02.25; UPC: 4061459716313
Codes / lots: Lot#: 197940521
Quantity: 150 cases
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
- Official notice
- FDA Enforcement Report, event 96951
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.