Ingredion Incorporated
Complete recall history across all FDA and CPSC categories — 4 total recalls
Ingredion Incorporated appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.
Food Recalls (4)
FDA food safety enforcement actions by Ingredion Incorporated
| Date | Product | Reason | Class |
|---|---|---|---|
| Oct 29, 2021 | Ingredion INSTANT PURE-FLO F (50 pound bag) food grade starch material 12151... | Potential for metal fragments in product | Class II |
| Oct 7, 2021 | Ingredion INSTANT PURE-FLOW F Food Starch, 50lb bag, material 12151103CA | Potential metal fragments in product | Class II |
| Jan 7, 2020 | Ingredion ULTRA-TEX4 Food Starch in 50lb paper bags, product code 32166102CA | Foreign material. Potential for fragments of stainless steel wire in the pro... | Class II |
| Feb 9, 2016 | Cornstach packaged in a 50lb. bag with white and green label containing black... | Food grade Cornstarch may contain metal fragments >1 mm in width and up to 50... | Class II |
Frequently Asked Questions
A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.
Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.
The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.
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