Food/Recall·openFDA/food

International Food Products Corporation — Class II: Dairy House Ingredient Systems Vanilla Dairy Powder, 50 lb box

MediumPublished Jun 24, 2026· AI-analyzed Jun 30, 2026View original FDA source
AI-generated regulatory interpretation. The four sections below are an analyst-style summary produced by an AI model from the original FDA source. Always verify against the source before any regulatory, clinical, or commercial decision.
What happened

International Food Products Corporation has initiated a Class II recall for its Dairy House Ingredient Systems Vanilla Dairy Powder (50 lb box) due to the potential presence of Salmonella.

Who it affects

This recall affects International Food Products Corporation, industrial food manufacturers utilizing vanilla dairy powder ingredients, and quality assurance personnel responsible for raw material sourcing.

Why it matters

A Class II recall indicates that the product may cause temporary or medically reversible adverse health consequences. For manufacturers using this ingredient, this event necessitates a traceability exercise to determine if contaminated raw materials have entered the production stream, which could lead to secondary recalls of finished goods. Although the source does not detail how the contamination was discovered, it underscores the ongoing risk of Salmonella in powdered dairy ingredients.

Practical takeaway

Regulatory and quality teams should immediately verify if any lots of this specific vanilla dairy powder are in their current inventory or have been integrated into finished products. QA should review supplier qualification records and ensure that pathogen testing protocols for raw ingredients are being strictly followed.

FDA source material

Class II. Reason: Potential for Salmonella. Product: Dairy House Ingredient Systems Vanilla Dairy Powder, 50 lb box. Firm: International Food Products Corporation (Hazelwood MO United States). Status: Ongoing.

Open in openFDA / FDA.gov
AI-generated interpretation. Always verify critical decisions against the original FDA source. Generated with google/gemini-3-flash-preview.