← FDA ENFORCEMENT
F-0298-2025Class II

Ocean Group Inc.

Recalling firm
Ocean Group Inc.
Product type
Food / supplement / cosmetic
Status
Terminated
Report date
2024-12-25
Distribution
Various retail and restaurant establishments in California.
Firm state
CA
Product quantity
5,925.91 Pounds total
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Environmental Monitoring
Reason for recall

Potential for contamination of Listeria monocytogenes. Environmental sample collected by FDA yielded positive results for one Zone 1 (cutting board) and one Zone 3 (floor drain).

Product description

SALMON BAKKAFROST FAROE ISLANDS 5/6KG FR FRO F LB SALMON NORWAY 6/7KG FR NOR F LB SALMON BAKKAFROST FAROE ISLANDS 6/7KG FR FRO F LB SALMON HIDDENFJORD FAROE ISLANDS 6/7KG FR F LB SALMON BAKKAFROST FAROE ISLANDS 7/8KG FR FRO F LB SALMON HIDDENFJORD FAROE ISLANDS 7/8KG FR F LB SALMON BAKKAFROST FAROE ISLANDS 8/9KG FR FRO F LB SALMON HIDDENFJORD FAROE ISLANDS 8/9KG FR F LB SALMON CANADA 12/14 FR CAN F LB SALMON CANADA 14/16 FR CAN F LB

Code / lot info

SALMON BAKKAFROST FAROE ISLANDS 5/6KG FR FRO F LB --- Lot SOLA-114464 SALMON NORWAY 6/7KG FR NOR F LB --- Lot INV 1374 SALMON BAKKAFROST FAROE ISLANDS 6/7KG FR FRO F LB --- Lot SOLA-114464 SALMON HIDDENFJORD FAROE ISLANDS 6/7KG FR F LB --- Lot F-142784 SALMON BAKKAFROST FAROE ISLANDS 7/8KG FR FRO F LB --- Lot SOLA-114485 SALMON HIDDENFJORD FAROE ISLANDS 7/8KG FR F LB --- Lot F-142784 SALMON BAKKAFROST FAROE ISLANDS 8/9KG FR FRO F LB --- Lot SOLA-114485 SALMON HIDDENFJORD FAROE ISLANDS 8/9KG FR F LB --- Lot F-142784 SALMON CANADA 12/14 FR CAN F LB --- Lot TNS349213 SALMON CANADA 14/16 FR CAN F LB --- Lot TNS349213

Other recalls SPEQ maps to Environmental Monitoring
2026-07-22Class IArgon Medical Devices, Inc2026-07-22Class IIOlympus Corporation of the Americas2026-07-22Class IIChiesi USA, Inc.2026-07-22Class IICareFusion 213, LLC
See all Environmental Monitoring recalls →

Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.