Class IITerminatedVoluntary: Firm initiated
International Food Products Corporation: food recall H-1076-2026
International Food Products Corporation of Hazelwood, MO recalled Legacy Tex Dressing Stabilizer Blend #7604-50, 50lb bags. Reason: Product tested positive for Salmonella. The FDA listed it as Class II in its Enforcement Report dated Jun 24, 2026; distribution: Oklahoma, Tennessee, Texas.
Record status as published: Terminated (terminated Sep 3, 2026). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- Legacy Tex Dressing Stabilizer Blend #7604-50, 50lb bags
- Product quantity
- 546 bags
- Reason for recall
- Product tested positive for Salmonella
- Codes, lots and dates on the package
- Lot 26121A6A Item #502574 Use by 2027-05-04
- Distribution pattern
- TX, TN, OK
- Recalling firm
- International Food Products Corporation, Hazelwood, MO
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | May 18, 2026 |
| Classified by the FDA | Jun 18, 2026 |
| Published in the Enforcement Report | Jun 24, 2026 |
| Terminated | Sep 3, 2026 |
Other products in the same recall event
The FDA groups related products under one recall event (event 99018).
- H-1078-2026 — Dairy House Ingredient Systems Strawberry Dairy Powder 05#5072-50, 50 lb bags
- H-1077-2026 — Dairy House Ingredient Systems Vanilla Dairy Powder, 50 lb box
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OpenPlate shows FDA records as published and does not add new findings. Product names and company names belong to their owners.
Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-1076-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.