FDA recall record

ISF "USA" High Liner Foods, Lightly Breaded Cod Tail Portions 4 oz recall — FDA F-2271-2017

The firm has decided to recall various products due to undeclared milk.

Class Iclassification
F-2271-2017official record ID
Jun 14, 2017report date

Recall record at a glance

Official recordF-2271-2017
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmISF "USA", LLC
Report dateJun 14, 2017
Recall initiation dateMay 12, 2017
Quantity2244 Cases
LocationNewport News, VA, United States

Official product description

High Liner Foods, Lightly Breaded Cod Tail Portions 4 oz. and 5 oz

Why the product was recalled

The firm has decided to recall various products due to undeclared milk.

Distribution information

All customers are within the United States.

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.