Westchester, IL, United States
Ingredion Incorporated recalls
4 recalls recorded since 2018, most recently on 29 October 2021. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls4
Ongoing (FDA)0
Terminated or completed4
Class I (FDA)0
Terminated Class II Food
- Recall started
- 29 October 2021
- Terminated
- 15 August 2025
- Reason
- Potential for metal fragments in product
- Distribution
- Distributors and manufacturers in: AR, CA, GA, IL, KY, MA, MI, MO, NC, NJ, NY, OH, PA, TX, WA, WI, CANADA, COLUMBIA, MEXICO
- Initiated
- Voluntary: Firm initiated
- Recall number
- F-0135-2022
- Ingredion INSTANT PURE-FLO F (50 pound bag) food grade starch material 12151103CA
Terminated Class II Food
- Recall started
- 7 October 2021
- Terminated
- 6 August 2025
- Reason
- Potential metal fragments in product
- Distribution
- Domestic: IN, OH, NJ International: CANADA, MEXICO, GUATEMALA
- Initiated
- Voluntary: Firm initiated
- Recall number
- F-0027-2022
- Ingredion INSTANT PURE-FLOW F Food Starch, 50lb bag, material 12151103CA
Terminated Class II Food
- Recall started
- 6 August 2021
- Terminated
- 10 June 2022
- Reason
- Undeclared egg allergen
- Distribution
- Distributed in the following states: CA, MA, FL, WA, UT, TX, ID, CT, IL, and SC.
- Initiated
- Voluntary: Firm initiated
- Recall number
- F-0956-2021
- Fermentation Derived Pepsin Product packaging: 5 individual LDPE bags with a net weight of 5kg each and 2.5kg sample bags packaged in 25 kg HDPE Drums
Terminated Class II Food
- Recall started
- 7 January 2020
- Terminated
- 23 January 2023
- Reason
- Foreign material. Potential for fragments of stainless steel wire in the product. Fragments are approximately 0.19mm in diameter with varying lengths of 1mm 20mm in length.
- Distribution
- CA, GA, IL, MN, MO, NC, NJ, OH Australia, Columbia, Indonesia, Vietnam
- Initiated
- Voluntary: Firm initiated
- Recall number
- F-0572-2020
- Ingredion ULTRA-TEX4 Food Starch in 50lb paper bags, product code 32166102CA
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.