International Food Products Corporation FDA recall records
The FDA has published 6 food recall enforcement records naming International Food Products Corporation between 2020 and 2026, covering 2 separate recall events. The firm is recorded in Missouri. Data last updated 2 September 2026.

- Records of 29,386
- 6
- Share of all recalls
- 0%
- Class I of 6
- 0
- Reported between
- 2020 to 2026
What these records are
Every record on this page was published by the FDA in the openFDA food enforcement database. 6 records cover 2 recall events, because the agency opens one record per product code: a single recall of a product line with many codes appears here many times.
0 of these records are Class I, 6 Class II and 0 Class III. A recall count is not a safety score. Most FDA food recalls are initiated by the firm itself, and a recall is the firm removing product from the market, which is what a food safety plan is built to produce.
What was recalled for
A single record can name more than one hazard, so these counts overlap.
By year
Counts are by the date the FDA reported the enforcement action. That date runs behind the date a firm started a recall, so the most recent year is always partial.
Where the recalling firms are
The state is the location of the recalling firm, not where the product was sold. Distribution is recorded separately on each record.
Most recently reported
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2026-06-24 | Dairy House Ingredient Systems Vanilla Dairy Powder, 50 lb box | International Food Products Corporation | Potential for Salmonella | Class II |
| 2026-06-24 | Legacy Tex Dressing Stabilizer Blend #7604-50, 50lb bags | International Food Products Corporation | Product tested positive for Salmonella | Class II |
| 2026-06-24 | Dairy House Ingredient Systems Strawberry Dairy Powder 05#5072-50, 50 lb bags | International Food Products Corporation | Potential for Salmonella | Class II |
| 2020-03-18 | Profile Food Ingredients, 10# Choc Dairy Pwd PFI-1010, packaged in 50 lb bags. | International Food Products Corporation | The firm received an ingredient that may have been contaminated with metal fragments and further manufactured and distributed products made with that ingredient. | Class II |
| 2020-03-18 | Dairy House Ingredients Systems, Anti-Sticking Starch Blend #9400-50 (501876) packaged in 50 lb bags | International Food Products Corporation | The firm received an ingredient that may have been contaminated with metal fragments and further manufactured and distributed products made with that ingredient. | Class II |
| 2020-03-18 | Dairy House Ingredients Systems, Chocolate Dairy Powder, 13# 50-91-0089, (501761) 39 packaged in 39 lb bags | International Food Products Corporation | The firm received an ingredient that may have been contaminated with metal fragments and further manufactured and distributed products made with that ingredient. | Class II |
Questions
- How many FDA recalls has International Food Products Corporation had?
- The FDA has published 6 food recall enforcement records naming International Food Products Corporation between 2020 and 2026. Those records cover 2 separate recall events: the agency opens one record per product code, so one recall of a product line appears as many records.
- Does a high recall count mean a firm is unsafe?
- Not on its own. Most FDA food recalls are initiated voluntarily by the firm, and a recall is the firm removing product from the market, which is what a working food safety plan is supposed to produce. Record counts also scale with the number of product codes a firm carries rather than with the number of things that went wrong.
A recall is the end of an evidence trail that either existed or did not. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.