CLASS II Food recall · Reported 24 Jun 2026 · FDA Enforcement Report

Legacy Tex Dressing Stabilizer Blend #7604 recalled

International Food Products is recalling Legacy Tex Dressing Stabilizer Blend #7604-50, distributed in Oklahoma, Tennessee, Texas. The recall was initiated on 18 May 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot 26121A6A Item #502574 Use by 2027-05-04
Quantity recalled546 bags

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-1076-2026
FDA event ID
99018
Recalling firm
International Food Products, Hazelwood, MO
Classification
Class II
Status
Terminated
Recall initiated
18 May 2026
FDA classified
18 Jun 2026
Reported
24 Jun 2026
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Salmonella
Product category
Sauces & Condiments

Timeline

18 May 2026Recall initiated by company
18 Jun 2026Classified by FDA+31 days
24 Jun 2026Published in enforcement report+6 days

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

Reason for recall

Product tested positive for 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

Legacy Tex Dressing Stabilizer Blend #7604-50, 50lb bags

Where it was distributed

TX, TN, OK

OklahomaTennesseeTexas

Questions about this recall

Why was it recalled?

Product tested positive for Salmonella

Which lots are affected?

Lot 26121A6A Item #502574 Use by 2027-05-04

Where was it sold?

TX, TN, OK

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

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.

Other products in this recall event

2 other products · FDA event 99018

This product is part of a recall event; the main page for the event is Dairy House Ingredient Systems Vanilla Dairy Powder recalled.

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