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Oregon Lox Company Recall: Listeria monocytogenes.

United States

TerminatedClass I

Company
Oregon Lox Company
Product
North Coast Smoked Salmon Trim - Partial Slices of Cold Smok…
Recall date
November 11, 2021
Terminated
December 16, 2021
Source
FDA

Reason for recall

Listeria monocytogenes.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
North Coast Smoked Salmon Trim - Partial Slices of Cold Smoked Salmon, net wt. 3 lb. UPC 008603002551. The Ingredients statement on the label are read in parts: "***INGREDIENTS: Salmon, salt, brown sugar, sodium nitrite, FD&C Yellow 6/Red 40, natural hardwood smoke ***CONTAINS: Keta Salmon (Fish) ***KEEP FROZEN OR STORE BELOW 38F ***". 008603002551 60 lbs. 22821

Distribution

  • distributed in AK
  • CA
  • OR
  • and WA.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0245-2022
Event ID
89038
Status
Terminated
Classification
Class I
Company
Oregon Lox Company
Product description
North Coast Smoked Salmon Trim - Partial Slices of Cold Smoked Salmon, net wt. 3 lb. UPC 008603002551. The Ingredients statement on the label are read in parts: "***INGREDIENTS: Salmon, salt, brown sugar, sodium nitrite, FD&C Yellow 6/Red 40, natural hardwood smoke ***CONTAINS: Keta Salmon (Fish) ***KEEP FROZEN OR STORE BELOW 38F ***".
Quantity
60 lbs.
Reason
Listeria monocytogenes.
Recall initiation date
November 11, 2021
Report date
December 15, 2021
Classification date
Not published in this source record
Termination date
December 16, 2021
Distribution pattern
distributed in AK, CA, OR, and WA.
UPC, lot, and code information
UPC 008603002551; 22821
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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 89038 with 2 other product entries in Public Health Trace.

FDA Recall United States Terminated Historical recordClass I

Oregon Lox Company

Product
Aqua Nova - Sliced Nova Lox, Oregon Cold Smoked Salmon, net…
Published
December 15, 2021
Distribution
distributed in AK, CA, OR, and WA.

View recall →

FDA Recall United States Terminated Historical recordClass I

Oregon Lox Company

Product
North Coast Traditional Nova Lox, cold smoked salmon, variou…
Published
December 15, 2021
Distribution
distributed in AK, CA, OR, and WA.

View recall →

Responsible company: Oregon Lox Company

Other recalls from Oregon Lox Company

FDA Recall United States Terminated Historical recordClass I

Oregon Lox Company

Product
Aqua Nova - Sliced Nova Lox, Oregon Cold Smoked Salmon, net…
Published
December 15, 2021
Distribution
distributed in AK, CA, OR, and WA.

View recall →

FDA Recall United States Terminated Historical recordClass I

Oregon Lox Company

Product
North Coast Traditional Nova Lox, cold smoked salmon, variou…
Published
December 15, 2021
Distribution
distributed in AK, CA, OR, and WA.

View recall →

Distribution map

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.

Distribution map
State Distributed
Alaska 1
California 1
Oregon 1
Washington 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.