RecallHawk
Class I Recall

Bulk WN-976-782-1 Seasoning for Cheese Sauce, Net Wt. 43.50 lbs., in a brown kraft bag

Givaudan Flavors Corp

Summary

The FDA issued a Class I for Bulk WN-976-782-1 Seasoning for Cheese Sauce, Net Wt. 43.50 lbs., in a brown kra by Givaudan Flavors Corp. Reason: Product has the potential to be contaminated with Salmonella..

Details

Source

Food Recall

External ID

H-0837-2026

Action Date

2026-05-13

Status

Ongoing

Category

food

Product Description

Bulk WN-976-782-1 Seasoning for Cheese Sauce, Net Wt. 43.50 lbs., in a brown kraft bag

Lot/Code Info: Batch: CS00140785; Expiry Date: 26 SEP 2026

Quantity Affected: 24,012 lbs.

Reason for Recall

Product has the potential to be contaminated with Salmonella.

Distribution

1 manufacturer in MO

Type: Voluntary: Firm initiated

Recall Initiated: 2026-04-22

Company

Givaudan Flavors Corp

Cincinnati, OH

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

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 (Givaudan Flavors Corp) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Givaudan Flavors Corp have FDA actions?

This is the only FDA action we have on record for Givaudan Flavors Corp in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0837-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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