Loki Fish Company - Office Recall: Potential to be contaminated with Listeria monocytogenes.
United States
TerminatedClass I
- Company
- Loki Fish Company - Office
- Product
- Loki Fish Wild Keta Salmon Lox, packaged in a 4 oz. plastic…
- Recall date
- August 23, 2021
- Terminated
- January 13, 2022
- Source
- FDA
Reason for recall
Potential to be contaminated with Listeria monocytogenes.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Loki Fish Wild Keta Salmon Lox, packaged in a 4 oz. plastic pouch, sliced on a coated board, 24 packages to a case. UPC 92103 00111. The label is read in parts: LOKI FISH *** WILD KETA LOX *** Ingredients: Wild Keta salmon, honey, salt and spices *** PRODUCT OF USA *** KEEP REFRIGERATED BELOW 38F ***lokifish.com***SEATTLE WA***". | Not published in this source record | 237 packages | There are no best by dates on the package. |
Distribution
- distributed in Oregon and Washington.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1005-2021
- Event ID
- 88554
- Status
- Terminated
- Classification
- Class I
- Company
- Loki Fish Company - Office
- Product description
- Loki Fish Wild Keta Salmon Lox, packaged in a 4 oz. plastic pouch, sliced on a coated board, 24 packages to a case. UPC 92103 00111. The label is read in parts: LOKI FISH *** WILD KETA LOX *** Ingredients: Wild Keta salmon, honey, salt and spices *** PRODUCT OF USA *** KEEP REFRIGERATED BELOW 38F ***lokifish.com***SEATTLE WA***".
- Quantity
- 237 packages
- Reason
- Potential to be contaminated with Listeria monocytogenes.
- Recall initiation date
- August 23, 2021
- Report date
- September 22, 2021
- Classification date
- Not published in this source record
- Termination date
- January 13, 2022
- Distribution pattern
- distributed in Oregon and Washington.
- UPC, lot, and code information
- There are no best by dates on the package.
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Press Release
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Loki Fish Company - Office
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.
