Yellow Corn Flour #620
Reason Product could contain foreign objects (pliable blue plastic)
Yellow Corn Flour #600 Unenriched 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 #600 Unenriched, packaged in bulk and 50 lb bags
Quantity: 7,852.20 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: 600-02-12, 600-02-13, 600-02-14, 600-03-01, 600-03-11, 600-03-12, 600-03-13, 600-03-14, 600-03-15, 9071A4, 9071A5, 9072A1E, 9072A4, 9073A2, 9078A3, 9079A3E, 9080A2, 9080A3, 9080A6, 9081A1E, 9081A7E, 9082A1E, 9082A4
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-1311-2019 · 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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