CLASS I Food recall · Reported 6 Nov 2019 · FDA Enforcement Report

Nathan's Cold Smoked Wild Salmon per wholesale case recalled

Vita Food Products is recalling Nathan's Cold Smoked Wild Salmon per wholesale case, distributed in Massachusetts. The recall was initiated on 14 Oct 2019 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot code 113420619C Best Before 20121.01
Quantity recalled20 cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0087-2020
FDA event ID
84058
Recalling firm
Vita Food Products, Chicago, IL
Classification
Class I
Status
Terminated
Recall initiated
14 Oct 2019
FDA classified
29 Oct 2019
Reported
6 Nov 2019
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Listeria
Product category
Salmon

Timeline

14 Oct 2019Recall initiated by company
29 Oct 2019Classified by FDA+15 days
6 Nov 2019Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Product tested positive for Listeria monocytogenes

Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.

Product as listed by the FDA

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

Where it was distributed

Single wholesaler in MA

Massachusetts

Questions about this recall

Why was it recalled?

Product tested positive for Listeria monocytogenes

Which lots are affected?

Lot code 113420619C Best Before 20121.01

Where was it sold?

Single wholesaler in MA

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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