Skip to main content
High RiskFDAfda-F-0092-2020CHEMICAL EXPOSURE

Frozen, raw tuna steaks individually packed in 8 oz. vacuum packages. Sold in cardboard cases (10 Lbs. per case).

Category
Units Affected
850
Recall Date
September 30, 2019
Issuing Agency
Hazard
Chemical Exposure

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0092-2020.

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

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0092-2020.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Northern Fisheries Ltd. or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0092-2020.

Northern Fisheries Ltd.

FDA

About the U.S. Food and Drug Administration

The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

Visit FDA.gov →

📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

How to report to FDAFile a report at FDA

Northern Fisheries Ltd. Recall FAQ

Northern Fisheries Ltd. is the subject of a seafood safety report: Frozen, raw tuna steaks individually packed in 8 oz. vacuum packages. Sold in cardboard cases (10 Lbs. per case).. The notice was published on September 30, 2019 by the U.S. Food and Drug Administration (FDA). Approximately 850 units are potentially affected.