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Use caution Food recall · FDA · Published March 28, 2019

Iowa Corn Processors Yellow Corn Flour #600 Unenriched Recall: Foreign Objects Hazard

Iowa Corn Processors recalls Yellow Corn Flour #600 Unenriched (3/11/2019 - 3/22/2019) due to possible foreign objects. Consumers should check product lots and contact for remedy.

🇺🇸 FDA recall #F-1311-2019FoodIowa Corn Processors ›
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Recalling firmIowa Corn Processors20481 Sycamore Ave · Glidden, IA 51443-8821
✎ GovInfoNow plain-language explainer

Iowa Corn Processors is recalling Yellow Corn Flour #600 Unenriched from March 11-22, 2019, because it may contain pliable blue plastic. This could cause choking or injury if ingested. Read more at govinfonow.com/recall/17604-iowa-corn-processors-yellow-corn-flour-600-unenriched-recall-foreign.

Source Summary by GovInfoNow · govinfonow.com/recall/17604-iowa-corn-processors-yellow-corn-flour-600-unenriched-recall-foreign · Updated October 5, 2026 · FDA enforcement record: FDA #F-1311-2019

Cite this page

“Iowa Corn Processors Yellow Corn Flour #600 Unenriched Recall: Foreign Objects Hazard.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/17604-iowa-corn-processors-yellow-corn-flour-600-unenriched-recall-foreign. Based on FDA recall #F-1311-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1311-2019%22&limit=1).

The FDA announced on March 28, 2019, that Iowa Corn Processors is recalling Yellow Corn Flour #600 Unenriched because it could contain pliable blue plastic. The voluntary recall affects approximately 7,852 pounds of product distributed to distributors and processors in several states and internationally.

How to tell if you have it

  • Brand: Iowa Corn Processors
  • Product: Yellow Corn Flour #600 Unenriched
  • Packaging: Bulk and 50 lb bags
  • Manufacture dates: 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
  • Distribution: Distributors and processors in AR, CA, IL, LA, MA, MO, RI, TN, TX, WA and Trinidad

The hazard

The product could contain foreign objects, specifically pliable blue plastic. The FDA classified this as a Class II recall.

Context

GovInfoNow's records show other recent recalls of similar products include Dakota Honey Spreadable Spun Honey Jalapeno Recall (2026-04-04) and Gerber Arrowroot Biscuits Recall (2026-01-26). Woodland Gourmet Arrowroot Flour Recall occurred on 2026-01-16.

How to tell if you have this one

Check the product lot numbers on the packaging: 600-02-12 through 600-03-15, 9071A4, 9071A5, 9072A1E, and other listed codes. The product was manufactured between March 11 and 22, 2019.

  • Brand
    Iowa Corn Processors
  • Category
    Food
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Terminated
  • Distribution
    Distributed to distributors and processors in AR, CA, IL, LA, MA, MO, RI, TN, TX, WA and internationally to Trinidad
Recall numberProduct, codes & lotsQuantity
F-1310-2019Yellow Corn Flour #620, Unenriched, packaged in bulk and 50 lb bags; 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, RS019035414,038.40 lbs
F-1311-2019Yellow Corn Flour #600 Unenriched, packaged in bulk and 50 lb bags; 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, 9082A47,852.20 lbs
Based on the official FDA remedy

What to do — step by step

  1. Check Product Lot Numbers

    Look for lot numbers on the packaging: 600-02-12 through 600-03-15, 9071A4, 9071A5, 9072A1E, and other listed codes.

Where it went and when

Where it was distributed

Distributed in 10 states, and outside the U.S.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: yesRIMassachusetts: yesMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: yesMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: yesARTennessee: yesTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: yesLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: yesTXFlorida: not listedFL

FDA distribution: “Distributed to distributors and processors in AR, CA, IL, LA, MA, MO, RI, TN, TX, WA and internationally to Trinidad” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arkansas, California, Illinois, Louisiana, Massachusetts, Missouri, Rhode Island, Tennessee, Texas, Washington.

Recall timeline

FDA terminated this recall 6 months after the firm started it.

1. Firm started the recall: Mar 28, 201912. FDA classified it Class II: Apr 30, 201923. Published in FDA’s Enforcement Report: May 8, 201934. FDA terminated the recall: Sep 24, 201942019
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-1311-2019 (March 28, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1311-2019 to see it in context.
  • Plain-language summary written by qwen3:4b on October 5, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA