CLASS I Food recall · Reported 19 Apr 2023 · FDA Enforcement Report

Biltmore Smoked Sockeye Salmon recalled by Seven Seas International USA

Seven Seas International USA is recalling Biltmore Smoked Sockeye Salmon. The recall was initiated on 13 Mar 2023 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLOT CODE: R4058 EXPIRATION DATE: 03-31-2024
Quantity recalled295 cases of 10 sleeves of 4oz

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-0708-2023
FDA event ID
91962
Recalling firm
Seven Seas International USA, Saint Petersburg, FL
Classification
Class I
Status
Terminated
Recall initiated
13 Mar 2023
FDA classified
11 Apr 2023
Reported
19 Apr 2023
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Listeria
Product category
Salmon

Timeline

13 Mar 2023Recall initiated by company
11 Apr 2023Classified by FDA+29 days
19 Apr 2023Published 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

Potential contamination with 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

Biltmore Smoked Sockeye Salmon - 4 oz

Where it was distributed

Domestic distribution only.

Questions about this recall

Why was it recalled?

Potential contamination with Listeria monocytogenes.

Which lots are affected?

LOT CODE: R4058 EXPIRATION DATE: 03-31-2024

Where was it sold?

Domestic distribution only.

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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