FDA recall record

Pier Fish Company Frozen Ground Tuna recall — FDA F-1513-2017

Elevated histamine levels.

Class IIclassification
F-1513-2017official record ID
Feb 22, 2017report date

Recall record at a glance

Official recordF-1513-2017
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmPier Fish Company, Inc.
Report dateFeb 22, 2017
Recall initiation dateJan 13, 2017
Quantity34 cases
LocationNew Bedford, MA, United States

Official product description

Frozen Ground Tuna. Product is labeled in part: "PIER FISH CO. 68 CONWAY ST NEW BEDFORD, MA 02740 COLUMBUS FISH & SFD TUNA GRIND LOT# 16185 PRODUCT OF : USA HARVESTED: WILD CAUGHT NET WT: 20 LBS

Why the product was recalled

Elevated histamine levels.

Distribution information

MA and OH

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA 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.