Ingredion INSTANT PURE-FLOW F Food Starch, 50lb bag, material 12151103CA
Summary
The FDA issued a Class II for Ingredion INSTANT PURE-FLOW F Food Starch, 50lb bag, material 12151103CA by Ingredion Incorporated. Reason: Potential metal fragments in product.
Details
Source
Food Recall
External ID
F-0027-2022
Action Date
2021-10-27
Status
Terminated
Category
food
Product Description
Ingredion INSTANT PURE-FLOW F Food Starch, 50lb bag, material 12151103CA
Lot/Code Info: Batches: CK2553 CK2555 DKI0185 DKI0189
Quantity Affected: 5,163 (qty.) 50 lb. bags
Reason for Recall
Potential metal fragments in product
Distribution
Domestic: IN, OH, NJ International: CANADA, MEXICO, GUATEMALA
Type: Voluntary: Firm initiated
Recall Initiated: 2021-10-07
Company
Westchester, IL
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 58 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Ingredion Incorporated has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Ingredion Incorporated) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Ingredion Incorporated have FDA actions?
Ingredion Incorporated has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0027-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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