Class IITerminated in FDA datasetRecall initiated Sep 30, 2019

Frozen, raw tuna loins packed in vacuum packages weighing between 5-8 Lbs. each. Packed in…

Recalling firm: Northern Fisheries Ltd.

Why it was recalled

Northern Fisheries Ltd. was notified by two of their customers that they received several consumer complaints from consumers who experienced symptoms of scombroid (histamine)…

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Mar 25, 2020.

Check your package

Compare the exact product and package details with the label you have.

ProductFrozen, raw tuna loins packed in vacuum packages weighing between 5-8 Lbs. each. Packed in cardboard cases (30 Lbs. per case).
Package size8 Lbs
UPC815838020621

FDA code information

Lot # 0058796 UPC # 815838020621 Production date: 6/13/2019 Best if used by date: 6/13/2021

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Frozen, raw tuna loins packed in vacuum packages weighing between 5-8 Lbs. each. Packed in cardboard cases (30 Lbs. per case).

Extracted codes and context

TypeCode / valueContext
UPC815838020621Lot # 0058796 UPC # 815838020621 Production date: 6/13/2019 Best if used by date: 6/13/2021
lot0058796Lot # 0058796 UPC # 815838020621 Production date: 6/13/2019 Best if used by date: 6/13/2021

Original FDA recall reason

Northern Fisheries Ltd. was notified by two of their customers that they received several consumer complaints from consumers who experienced symptoms of scombroid (histamine) poisoning after consuming tuna steaks distributed by Northern Fisheries Ltd.

Recall details

Recall number
F-0093-2020
Event ID
83933
FDA status
Terminated
Initiated
Sep 30, 2019
Reported
Oct 23, 2019
Classified
Oct 30, 2019
Terminated
Mar 25, 2020
Quantity
345 cases (10,350 Lbs.)
Location
Little Compton, RI, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

GA, PA, MD, MN, & VA

FDA source record · F-0093-2020

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.