FDA Recall United States Terminated Historical recordClass I
Ocean Group Inc.
- Product
- 202225 SALMON BAKKA FROST FILLET 6/7KG FR FRO F LB 202002 S…
- Published
- February 7, 2024
- Distribution
- U.S. distribution: CA No foreign distri…
Ocean Group Inc. Recall: Potential L. mono contamination as a result of FDA environmental sampling revealing positive findings.
United States
TerminatedClass I
- Company
- Ocean Group Inc.
- Product
- 201000 TUNA, HAWAII #1 USA W LB 201002 TUNA HAWAII #1 USA W…
- Recall date
- December 29, 2023
- Terminated
- June 14, 2024
- Source
- FDA
Reason for recall
Potential L. mono contamination as a result of FDA environmental sampling revealing positive findings.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 201000 TUNA, HAWAII #1 USA W LB 201002 TUNA HAWAII #1 USA W LB 201200 TUNA FRESH, WILD Y/F,B/E #2 GRADE 201300 TUNA BLUEFIN SPAIN SPA F LB 201301 TUNA BLUEFIN SPAIN (SE) SPAIN F LB 201304 TUNA BLUEFIN SPAIN G&G SPAIN F LB 201508 TUNA BLUE FIN GG JAPAN FR JPN F LB 201900 TUNA, FRESH SCRAPS "TESSHIN" WILD LB TUNA001B TUNA, FRESH "BLUEFINA" MEXICO FARM LB TUNA001C TUNA, FRESH TUNA BLUEFIN PORTION (MEXICO) FARM/LB TUNA001D TUNA BLUE FIN MEXICO SMALL FR MEX FLB TUNA001E TUNA BLUE FIN *BACKSIDE* MEXICO FARM LB TUNA001NZ TUNA, BLUE FIN LOCAL WILD LB TUNA001W TUNA, FRESH BOSTON BLUEFIN WILD LB | Not published in this source record | 166 pieces | Expiration date: Dec 11-Dec 29 |
Distribution
- U.S. distribution: CA No foreign distribution.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0805-2024
- Event ID
- 93716
- Status
- Terminated
- Classification
- Class I
- Company
- Ocean Group Inc.
- Product description
- 201000 TUNA, HAWAII #1 USA W LB 201002 TUNA HAWAII #1 USA W LB 201200 TUNA FRESH, WILD Y/F,B/E #2 GRADE 201300 TUNA BLUEFIN SPAIN SPA F LB 201301 TUNA BLUEFIN SPAIN (SE) SPAIN F LB 201304 TUNA BLUEFIN SPAIN G&G SPAIN F LB 201508 TUNA BLUE FIN GG JAPAN FR JPN F LB 201900 TUNA, FRESH SCRAPS "TESSHIN" WILD LB TUNA001B TUNA, FRESH "BLUEFINA" MEXICO FARM LB TUNA001C TUNA, FRESH TUNA BLUEFIN PORTION (MEXICO) FARM/LB TUNA001D TUNA BLUE FIN MEXICO SMALL FR MEX FLB TUNA001E TUNA BLUE FIN *BACKSIDE* MEXICO FARM LB TUNA001NZ TUNA, BLUE FIN LOCAL WILD LB TUNA001W TUNA, FRESH BOSTON BLUEFIN WILD LB
- Quantity
- 166 pieces
- Reason
- Potential L. mono contamination as a result of FDA environmental sampling revealing positive findings.
- Recall initiation date
- December 29, 2023
- Report date
- February 7, 2024
- Classification date
- Not published in this source record
- Termination date
- June 14, 2024
- Distribution pattern
- U.S. distribution: CA No foreign distribution.
- UPC, lot, and code information
- Expiration date: Dec 11-Dec 29
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Letter
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 93716 with 1 other product entry in Public Health Trace.
Responsible company: Ocean Group Inc.
Other recalls from Ocean Group Inc.
FDA Recall United States Terminated Historical recordClass II
Ocean Group Inc.
- Product
- SALMON BAKKAFROST FAROE ISLANDS 5/6KG FR FRO F LB SALMON NOR…
- Published
- December 25, 2024
- Distribution
- Various retail and restaurant establishm…
FDA Recall United States Terminated Historical recordClass I
Ocean Group Inc.
- Product
- 202225 SALMON BAKKA FROST FILLET 6/7KG FR FRO F LB 202002 S…
- Published
- February 7, 2024
- Distribution
- U.S. distribution: CA No foreign distri…
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| California | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
