FDA recall record

B & I Overseas Trading Herring in Oil with Italian Spices: Ingredients: Herring recall — FDA F-0202-2021

Washington State Department of Agriculture samples product and had a positive result of Listeria monocytogenes.

Class Iclassification
F-0202-2021official record ID
Jan 20, 2021report date

Recall record at a glance

Official recordF-0202-2021
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmB & I Overseas Trading Inc.
Report dateJan 20, 2021
Recall initiation dateDec 23, 2020
Quantity400 individual pieces
LocationVan Nuys, CA, United States

Official product description

Herring in Oil with Italian Spices: Ingredients: Herring fillet pieces (fish) sunflower oil refined deodorized, edible salt, ground spices (chili, mustard, coriander, acidity regulators: acetic acid, glucono-delta-lactone; antioxidants; dihdroxysuccinic acid, citric acid, d-glucose, glucose syrup solution,, preserving agents: potassium sorbate, sodium benzoate: Contains: fish NET WEIGHT 17.74 oz. (500g) Storage conditions: keep at temperature below 0 degrees F to date of Best Before. Product of Ukraine UPC: 40823097 903896 Importer: B&I Overseas Trading, Inc., Van Nuys, CA www bioverseas.com

Why the product was recalled

Washington State Department of Agriculture samples product and had a positive result of Listeria monocytogenes.

Distribution information

U.S distribution to the following: WA No foreign distribution.

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.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.