RecallHawk
Class I Recall

Frozen, Lightly Seasoned Salmon Burgers, 28x6oz., 10.5 lbs cases

Raw Seafoods Inc.

Summary

The FDA issued a Class I for Frozen, Lightly Seasoned Salmon Burgers, 28x6oz., 10.5 lbs cases by Raw Seafoods Inc.. Reason: Contains undeclared sesame seeds and milk.

Details

Source

Food Recall

External ID

F-0622-2024

Action Date

2023-12-27

Status

Terminated

Category

food

Product Description

Frozen, Lightly Seasoned Salmon Burgers, 28x6oz., 10.5 lbs cases

Lot/Code Info: Lot: B5589 PLU 56228 Model, catalog, or product order numbers: V10200D, DZZBGR9006

Quantity Affected: 9019 lbs (859 cases)

Reason for Recall

Contains undeclared sesame seeds and milk

Distribution

Nationwide

Type: Voluntary: Firm initiated

Recall Initiated: 2023-11-15

Company

Raw Seafoods Inc.

Fall River, MA

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 157 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Raw Seafoods Inc. has 3 FDA actions in our database, including 3 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 (Raw Seafoods Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Raw Seafoods Inc. have FDA actions?

Raw Seafoods Inc. has 3 FDA actions in our database, including 3 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0622-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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