Food Recall Check
Class II · Moderate risk Terminated Initiated Mar 28, 2019 (8 years ago)

Yellow Corn Flour #620 recall

Recalled by Iowa Corn Processors · Glidden, IA, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Product could contain foreign objects (pliable blue plastic)

Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.

What was recalled

Yellow Corn Flour #620, Unenriched, packaged in bulk and 50 lb bags

Quantity: 14,038.40 lbs

Food: Pasta, rice & grains

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Manufacture date range 3/11/2019 - 3/22/2019 Lots: 620-03-04, 620-03-05, 620-03-06, 620-03-07, 620-03-08, 620-03-09, 9071A6, 9071A7, 9072A2, 9073A4, 9074A1, 9075A1, 9075A5, 9078A1, 9078A8/9074A1, 9080A1, 9080A9/9078A1, 9082A5/9080A9, RS0190332, RS0190343, RS0190354

Where it was sold

Arkansas California Illinois Louisiana Massachusetts Missouri Rhode Island Tennessee Texas Washington

FDA's distribution note: Distributed to distributors and processors in AR, CA, IL, LA, MA, MO, RI, TN, TX, WA and internationally to Trinidad

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Iowa Corn Processors
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 28, 2019
In FDA report of
May 8, 2019
Terminated
Sep 24, 2019
FDA recall number
F-1310-2019 · event 82524
Official record
FDA enforcement report search

Also recalled with it (1 more product)

FDA files each product of one recall action separately; these share the same FDA event.

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