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Lower risk Food recall · FDA · Published March 11, 2019

Yost Foods Aji Amarillo Paste Recall: Listeria Contamination Risk

Yost Foods recalls 40-lb buckets of Aji Amarillo Paste (Lot Y05319) due to Listeria monocytogenes contamination. Consumers should avoid using this product to prevent potential foodborne illness.

🇺🇸 FDA recall #F-1309-2019FoodYost Foods ›
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Recalling firmYost Foods, Inc2795 Westway Dr · Brunswick, OH 44212-5708
✎ GovInfoNow plain-language explainer

Yost Foods is recalling 40-pound buckets of Aji Amar:illo Paste (Lot Y05319) because it tested positive for Listeria monocytogenes, a bacteria that can cause serious foodborne illness. This recall is important because Listeria can lead to infections that may be especially dangerous for pregnant women, newborns, and the elderly. Read more at govinfonow.com/recall/17657-yost-foods-aji-amarillo-paste-recall-listeria-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/17657-yost-foods-aji-amarillo-paste-recall-listeria-contamination-risk · Updated October 5, 2026 · FDA enforcement record: FDA #F-1309-2019

Cite this page

“Yost Foods Aji Amarillo Paste Recall: Listeria Contamination Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/17657-yost-foods-aji-amarillo-paste-recall-listeria-contamination-risk. Based on FDA recall #F-1309-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1309-2019%22&limit=1).

Yost Foods, Inc. recalled Aji Amarillo Paste distributed to one customer in Ohio after the product tested positive for Listeria monocytogenes, according to the FDA. The Food and Drug Administration announced the Class I recall on March 11, 2019.

How to tell if you have it

  • Brand: Yost Foods
  • Product: Aji Amarillo Paste
  • Packaging: 40 lb buckets
  • Lot code: Y05319
  • Quantity: 1000 lbs

The hazard

The product tested positive for Listeria monocytogenes. The FDA classified the recall as Class I, indicating a reasonable probability that the use of or exposure to the product will cause serious adverse health consequences or death.

Context

GovInfoNow's records show other recent recalls involving Listeria contamination risks include Gias Food Lemon Alfredo Fettuccine (2026-09-03), Made Fresh Salads Jalapeno Cream Cheese (2026-02-19), and Clover Hill Dairy Soft Cuajada in Brine (2026-06-01).

How to tell if you have this one

Check for the product name 'Aji Amarillo Paste' in 40-lb buckets. The specific lot number is Y05319. This product was sold by Yost Foods.

  • Brand
    Yost Foods
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the lot number Y05319 on the 40-lb bucket of Aji Amarillo Paste.

Where it went and when

Where it was distributed

Distributed in Ohio.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew 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: not listedNCSouth 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: “Distributed to one customer in Ohio.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Ohio.

Recall timeline

FDA terminated this recall 10 months after the firm started it.

1. Firm started the recall: Mar 11, 201912. FDA classified it Class I: Apr 26, 201923. Published in FDA’s Enforcement Report: May 8, 201934. FDA terminated the recall: Dec 27, 201942019
  1. Firm started the recall
  2. FDA classified it Class I
  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-1309-2019 (March 11, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1309-2019 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