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Stop using now Food recall · FDA · Published March 8, 2018

ADM Provim ESP Vita Wheat Gluten Recall: Listeria Contamination Risk

ADM recalls Provim ESP Vita Wheat Gluten (50 lb bags) due to Listeria monocytogenes contamination. Consumers should avoid using these products to prevent potential foodborne illness.

🇺🇸 FDA recall #F-1099-2018FoodADM Agri Industries ›
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Recalling firmADM Agri Industries155 D'Iberia Ave · Candiac, Canada
✎ GovInfoNow plain-language explainer

What happened, in plain English

ADM Agri Industries is recalling Provim ESP Vita Wheat Gluten (50 lb bags) because the flour used in production tested positive for Listeria monocytogenes. This bacteria can cause serious foodborne illness, so affected consumers should stop using the product. Read more at govinfonow.com/recall/19592-adm-provim-esp-vita-wheat-gluten-recall-listeria-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/19592-adm-provim-esp-vita-wheat-gluten-recall-listeria-contamination-risk · Updated October 7, 2026 · FDA enforcement record: FDA #F-1099-2018

Cite this page

“ADM Provim ESP Vita Wheat Gluten Recall: Listeria Contamination Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19592-adm-provim-esp-vita-wheat-gluten-recall-listeria-contamination-risk. Based on FDA recall #F-1099-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1099-2018%22&limit=1).

Why it’s dangerous

Listeria monocytogenes is a bacterium that can cause serious foodborne illness, including life-threatening infections. The contamination occurred during the manufacturing process, meaning the product could be unsafe for consumption even if it appears normal.

Who’s affected

Anyone who purchased Provim ESP Vita Wheat Gluten (50 lb bags) with the specific lot numbers listed in the recall. People with weakened immune systems are at higher risk for severe illness from Listeria.

How to tell if you have this one

Check for the product name 'Provim ESP Vita Wheat Gluten', 50 lb bags, and lot numbers: 04087-(01-25)-C, 04287-40-C, 04387-40-C, or 04787-40-C. These products expire by February 9, 11, 13, or 16, 2019 respectively.

  • Brand
    ADM Agri Industries
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop Using Product

    Immediately stop using any Provim ESP Vita Wheat Gluten bags with the listed lot numbers as they may contain Listeria monocytogenes.

Where it went and when

Where it was distributed

Distributed in 5 states.

Alaska: not listedAKMaine: yesMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: not listedWIMichigan: yesMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: yesOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: yesNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “Product was shipped to the following states: IL, ME, MI, NC & OH.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Illinois, Maine, Michigan, North Carolina, Ohio.

Recall timeline

FDA terminated this recall 2.3 years after the firm started it.

1. Firm started the recall: Mar 8, 201812. FDA classified it Class II: Apr 16, 201823. Published in FDA’s Enforcement Report: Apr 25, 201834. FDA terminated the recall: Jul 9, 2020420182020
  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.

✎ GovInfoNow

Questions people ask

What should I do with the recalled product?

Discard the product immediately as it poses a health risk. Do not use it for any purpose.

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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-1099-2018 (March 8, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1099-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 7, 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