RecallHawk
Class I Recall

BrS8 RODIZIO Seas No MSG 9.6#, SAP Code: 20644205. Kerry Ingredients, 3400 Millington Road, Beloit, WI 53511

Kerry, Inc

Summary

The FDA issued a Class I for BrS8 RODIZIO Seas No MSG 9.6#, SAP Code: 20644205. Kerry Ingredients, 3400 Mi by Kerry, Inc. Reason: Potential Salmonella Contamination..

Details

Source

Food Recall

External ID

F-1354-2024

Action Date

2024-06-19

Status

Terminated

Category

food

Product Description

BrS8 RODIZIO Seas No MSG 9.6#, SAP Code: 20644205. Kerry Ingredients, 3400 Millington Road, Beloit, WI 53511

Lot/Code Info: Lot: 7913195.

Quantity Affected: 68 bags

Reason for Recall

Potential Salmonella Contamination.

Distribution

AZ, CA, GA, ID, IL, IN, KS, MD. Outside the US: Canada

Type: Voluntary: Firm initiated

Recall Initiated: 2024-05-03

Company

Kerry, Inc

Beloit, WI

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

Kerry, Inc has 6 FDA actions in our database, including 6 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 (Kerry, Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Kerry, Inc have FDA actions?

Kerry, Inc has 6 FDA actions in our database, including 6 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1354-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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