RecallHawk
Class I Recall

Biltmore Smoked Sockeye Salmon - 4 oz

Seven Seas International USA LLC

Summary

The FDA issued a Class I for Biltmore Smoked Sockeye Salmon - 4 oz by Seven Seas International USA LLC. Reason: Potential contamination with Listeria monocytogenes..

Details

Source

Food Recall

External ID

F-0708-2023

Action Date

2023-04-19

Status

Terminated

Category

food

Product Description

Biltmore Smoked Sockeye Salmon - 4 oz

Lot/Code Info: LOT CODE: R4058 EXPIRATION DATE: 03-31-2024

Quantity Affected: 295 cases of 10 sleeves of 4oz

Reason for Recall

Potential contamination with Listeria monocytogenes.

Distribution

Domestic distribution only.

Type: Voluntary: Firm initiated

Recall Initiated: 2023-03-13

Company

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 45 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Seven Seas International USA LLC has 2 FDA actions in our database, including 2 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Seven Seas International USA LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Seven Seas International USA LLC have FDA actions?

Seven Seas International USA LLC has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0708-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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