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FDA recall, , Moderate risk

International Food Products Dairy Powders and Dressing Stabilizer

Legacy Tex Dressing Stabilizer Blend tested positive for Salmonella, and Vanilla and Strawberry Dairy Powders have potential for Salmonella.

Recall ended Sep 3, 2026. Still check yours.

What happened

International Food Products Corporation of Hazelwood, Missouri recalled Dairy House Ingredient Systems Vanilla Dairy Powder, 50 lb box, Legacy Tex Dressing Stabilizer Blend #7604-50, 50lb bags, and Dairy House Ingredient Systems Strawberry Dairy Powder 05#5072-50, 50 lb bags, due to potential for Salmonella in the vanilla and strawberry powders and a positive test for Salmonella in the stabilizer blend.

The recall began May 18, 2026, and was added to the FDA's Enforcement Report on June 18, 2026, with distribution in Oklahoma, Tennessee and Texas.

What to do

We don't have product-specific instructions for this recall. FDA's general advice for food recalls:

  1. Return it to the store where you bought it, or throw it away.
  2. Don't give it to anyone else, such as a food bank, or to a pet.

Is yours affected?

3 products

Affected if its lot code is listed.

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

    Reason: Product tested positive for Salmonella

    Lot code
    • 26121A6A
    • 502574
    • 2027-05-04
  2. Dairy House Ingredient Systems Vanilla Dairy Powder, 50 lb box

    Reason: Potential for Salmonella

    Lot code
    • 26125A6B
    • 502269
    • 2027-05-05
  3. Dairy House Ingredient Systems Strawberry Dairy Powder 05#5072-50, 50 lb bags

    Reason: Potential for Salmonella

    Lot code
    • 26126A6A
    • 2027-05-06

Recall details

Company began the recall
Company
International Food Products CorporationHazelwood, Missouri
Risk

Moderate risk

Eating it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.

FDA Class II recall · How risk is rated

Event ID
99018
Recall numbers
H-1076-2026 to H-1078-2026

Timeline

FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.

  1. Company began the recall

  2. Added to FDA's Enforcement Report · Classified by FDA

  3. Listed on Recall Canary

  4. In FDA's weekly enforcement report

  5. Recall ended

  6. Summary updated

Summary by Recall Canary, written with AI · summary updated Oct 12, 2026 · primary source: U.S. Food and Drug Administration (opens in a new tab)