Skip to main content
CriticalFDAfda-F-0087-2020LISTERIA

NATHAN'S COLD SMOKED WILD SALMON, in 3oz.vacuum packed pouch, 12 units per wholesale case, UPC 73030 80686

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (listeria). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Category
Units Affected
20
Recall Date
October 14, 2019
Issuing Agency
Hazard
Listeria

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0087-2020.

Product tested positive for Listeria monocytogenes

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0087-2020.

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 Vita Food Products, Inc. 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-0087-2020.

Vita Food Products, Inc.

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

Vita Food Products, Inc. Recall FAQ

Vita Food Products, Inc. is the subject of a seafood safety report: NATHAN'S COLD SMOKED WILD SALMON, in 3oz.vacuum packed pouch, 12 units per wholesale case, UPC 73030 80686. The notice was published on October 14, 2019 by the U.S. Food and Drug Administration (FDA). Approximately 20 units are potentially affected.