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Stop using now Food recall · FDA · Published January 11, 2019

El Guapo Chile Pods Recall: Unlabeled Peanut Allergen

El Guapo Pasilla-Ancho Chile Pods are recalled due to unlabeled peanut allergen. Check UPCs and best-by dates for affected lots.

🇺🇸 FDA recall #F-1346-2019FoodEl Guapo ›
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Contact the company

Recalling firmMcCormick & Company, Inc. - Flavor Manufacturing Center11102 McCormick Rd Bldg 20 · Hunt Valley, MD 21031-1404
✎ GovInfoNow plain-language explainer

McCormick & Company, Inc., through its subsidiary Mojave Foods Corporation, is recalling El Guapo Pasilla-Ancho Chile Pods because they contain an unlabeled peanut allergen. This poses a risk to individuals with peanut allergies who may unknowingly consume the product. The recall covers specific lots distributed across multiple states. Read more at govinfonow.com/recall/17826-el-guapo-chile-pods-recall-unlabeled-peanut-allergen.

Source Summary by GovInfoNow · govinfonow.com/recall/17826-el-guapo-chile-pods-recall-unlabeled-peanut-allergen · Updated October 11, 2026 · FDA enforcement record: FDA #F-1346-2019

Cite this page

“El Guapo Chile Pods Recall: Unlabeled Peanut Allergen.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/17826-el-guapo-chile-pods-recall-unlabeled-peanut-allergen. Based on FDA recall #F-1346-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1346-2019%22&limit=1).

The FDA announced on Jan. 11, 2019, that McCormick & Company, Inc. - Flavor Manufacturing Center is recalling El Guapo Pasilla-Ancho Chile Pods due to an unlabeled peanut allergen hazard. The agency classified the recall as Class I.

How to tell if you have it

  • El Guapo Pasilla-Ancho Chile Pods 2oz, UPC# 044989010391, Best By Jun/20/20
  • El Guapo Pasilla-Ancho Chile Pods 7.5oz, UPC# 044989211088, Best By Jun/13/20 or Jun/14/20
  • El Guapo Pasilla-Ancho Chile Pods 11oz, UPC# 044989211149, Best By Jun/12/20

The hazard

Mojave Foods Corporation, a subsidiary of McCormick, initiated the voluntary recall because the El Guapo Chile Habanero and Chile Pasilla-Ancho pouches contain unlabeled peanut allergen.

Context

GovInfoNow's records show McCormick & Company, Inc. - Flavor Manufacturing Center has two other recalls on record since Sept. 10, 2018. Other recent recalls of similar products include Fayus OLA-OLA Pounded Groundnuts Recall (June 19, 2026), Wilco Peanut Co Raw Shelled Peanuts Recall (May 18, 2026), and High Valley Orchard Chocolate Covered Raisins Recall (June 24, 2026).

How to tell if you have this one

Check your pantry for El Guapo Pasilla-Ancho Chile Pods in pouches labeled as 2oz, 7.5oz, or 11oz. Verify the UPC codes: 044989010391 (2oz), 044989211088 (7.5oz), and 044989211149 (11oz). Check the 'Best By' dates, which include Jun/20/20, Jun/13/20, Jun/14/20, and Jun/12/20.

  • Brand
    El Guapo
  • Product
    El Guapo Pasilla-Ancho Chile Pods 2oz, 7.5oz, 11oz
  • 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 I
  • Status
    Terminated
  • Distribution
    Product distributed to the following states: AL, AR, AZ, CA, CO, FL, GA, ID, IL, IN, IA, KS, KY, MI, MN, MO, MT, NE, NV, NM, NC, OH, OK, OR, TN, TX, UT, WI
Recall numberProduct, codes & lotsQuantity
F-1345-2019El Guapo Chile Habanero Habanero Chili Pepper 0.5oz; UPC# 044989012968; Best By Apr/05/19; Best By; Jun/21/19; Best By Jun/22/19; Best By Oct/29/19; Best By Dec/07/19; Best By Feb/05/20; Best By Feb/06/20; Best By; Jun/12/2047,044 pouches
F-1346-2019El Guapo Pasilla-Ancho Chile Pods 2oz, 7.5oz, 11oz; 2oz: UPC# 044989010391; Best By Jun/20/20 7.5oz: UPC# 044989211088; Best By Jun/13/20; Best By Jun/14/20 11oz: UPC# 044989211149; Best By Jun/12/202 oz, 22,848 pouches ; 7.5oz, 13,896 pouches ; 11oz, 2,064 pouches
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat the recalled El Guapo Pasilla-Ancho Chile Pods due to the risk of an allergic reaction from unlabeled peanuts.

  2. Discard or return the item

    The record does not specify a return address or refund process, so you should discard the product safely.

Where it went and when

Where it was distributed

Distributed in 28 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: yesIDMontana: yesMTNorth Dakota: not listedNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: yesORNevada: yesNVWyoming: not listedWYSouth Dakota: not listedSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: yesOKLouisiana: not listedLAMississippi: not listedMSAlabama: yesALGeorgia: yesGAHawaii: not listedHITexas: yesTXFlorida: yesFL

FDA distribution: “Product distributed to the following states: AL, AR, AZ, CA, CO, FL, GA, ID, IL, IN, IA, KS, KY, MI, MN, MO, MT, NE, NV, NM, NC, OH, OK, OR, TN, TX, UT, WI” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Alabama, Arizona, Arkansas, California, Colorado, Florida, Georgia, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Michigan, Minnesota, Missouri, Montana, Nebraska, Nevada, New Mexico, North Carolina, Ohio, Oklahoma, Oregon, Tennessee, Texas, Utah, Wisconsin.

Recall timeline

FDA terminated this recall 5 months after the firm started it.

1. Firm started the recall: Jan 11, 201912. FDA classified it Class I: May 13, 201923. Published in FDA’s Enforcement Report: May 15, 201934. FDA terminated the recall: Jun 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-1346-2019 (January 11, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1346-2019 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 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