FDA recall record

Oregon Lox Company Aqua Nova - Sliced Nova Lox, Oregon Cold Smoked Salmon, net wt recall — FDA F-0243-2022

Listeria monocytogenes.

Class Iclassification
F-0243-2022official record ID
Dec 15, 2021report date

Recall record at a glance

Official recordF-0243-2022
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmOregon Lox Company
Report dateDec 15, 2021
Recall initiation dateNov 11, 2021
Quantity1294 lbs.
LocationEugene, OR, United States

Official product description

Aqua Nova - Sliced Nova Lox, Oregon Cold Smoked Salmon, net wt. 3 oz. UPC 008603001608. Aqua Nova -Sliced Nova Lox, Oregon Cold Smoked Salmon, net wt. 1 lb. UPC 008603001400. Aqua Nova - Premium Oregon Nova Lox (Sliced), cold smoked salmon, various net wt 2-3 lbs per side. UPC 008603001202. Aqua Nova - Premium Oregon Nova Lox (UnSliced), cold smoked salmon, various net wt. 2.5-3.5lb average per side. UPC 008603001103. Tony's Smoke House and Cannery - Smoked Salmon Lox, cold smoked - Nova Style - Presliced, net wt. 8oz. UPC 0086030015608. The Ingredients statement on these labels are read in parts: "***INGREDIENTS: Wild Pacific 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 ***".

Why the product was recalled

Listeria monocytogenes.

Distribution information

distributed in AK, CA, OR, and WA.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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