CLASS I Food recall · Reported 13 May 2026 · FDA Enforcement Report

Bulk WN-976-782-1 Seasoning for Cheese Sauce recalled

Givaudan Flavors is recalling Bulk WN-976-782-1 Seasoning for Cheese Sauce, distributed in Missouri. The recall was initiated on 22 Apr 2026 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBatch: CS00140785; Expiry Date: 26 SEP 2026
Quantity recalled24,012 lbs.

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
H-0837-2026
FDA event ID
98827
Recalling firm
Givaudan Flavors, Cincinnati, OH
Classification
Class I
Status
Terminated
Recall initiated
22 Apr 2026
FDA classified
21 May 2026
Reported
13 May 2026
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Salmonella
Product category
Sauces & Condiments

Timeline

22 Apr 2026Recall initiated by company
13 May 2026Published in enforcement report+21 days
21 May 2026Classified by FDA+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Product has the potential to be contaminated with Salmonella.

Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.

Product as listed by the FDA

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

Where it was distributed

1 manufacturer in MO

Missouri

Questions about this recall

Why was it recalled?

Product has the potential to be contaminated with Salmonella.

Which lots are affected?

Batch: CS00140785; Expiry Date: 26 SEP 2026

Where was it sold?

1 manufacturer in MO

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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