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Lower risk Food recall · FDA · Published November 20, 2024

Jose Madrid Salsa Chipotle Con Queso Recall: Undeclared Yellow Dyes

Recall of Jose Madrid Salsa Chipotle Con Queso (13oz glass jars) due to undeclared Yellow #5 and Yellow #6 dyes. Check lot numbers on jars for affected products.

🇺🇸 FDA recall #F-0252-2025FoodJose Madrid ›
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Contact the company

Recalling firmMichael Zakany LLC601 Putnam Ave · Zanesville, OH 43701-5504
✎ GovInfoNow plain-language explainer

What happened, in plain English

Jose Madrid is recalling its Chipotle Con Queso salsa in 13oz glass jars because it contains undeclared yellow dyes (Yellow #5 and Yellow #6). This could be a health risk for people sensitive to artificial dyes. Read more at govinfonow.com/recall/8589-jose-madrid-salsa-chipotle-con-queso-recall-undeclared-yellow-dyes.

Source Summary by GovInfoNow · govinfonow.com/recall/8589-jose-madrid-salsa-chipotle-con-queso-recall-undeclared-yellow-dyes · Updated August 17, 2026 · FDA enforcement record: FDA #F-0252-2025

Cite this page

“Jose Madrid Salsa Chipotle Con Queso Recall: Undeclared Yellow Dyes.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/8589-jose-madrid-salsa-chipotle-con-queso-recall-undeclared-yellow-dyes. Based on FDA recall #F-0252-2025 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0252-2025%22&limit=1).

Why it’s dangerous

The product contains undeclared Yellow #5 and Yellow #6 dyes, which are artificial colorants. These dyes can cause allergic reactions or other health issues in individuals sensitive to them, but the recall does not indicate a risk of serious injury.

Who’s affected

Owners of Jose Madrid Salsa Chipotle Con Queso in 13oz glass jars with lot numbers 601 22 01 102327, 601 22 01 103027, or 601 22 01 111227 are affected. People sensitive to artificial dyes may be at higher risk.

How to tell if you have this one

Check for glass jars labeled 'Jose Madrid Salsa Chipotle Con Queso, Net Wt. 13 oz. (369g)'. Look for lot numbers 601 22 01 102327, 601 22 01 103027, or 601 22 01 111227 on the jars.

  • Brand
    Jose Madrid
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Lot Number

    Look for lot numbers 601 22 01 102327, 601 22 01 103027, or 601 22 01 111227 on the glass jars.

Where it went and when

Where it was distributed

Distributed in 16 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: yesCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: yesVAMaryland: yesMDDelaware: 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: yesALGeorgia: yesGAHawaii: not listedHITexas: yesTXFlorida: yesFL

FDA distribution: “Product was sold through 6 distributors and direct internet sales to customers in AL, CO, FL, GA, IL, MD, MI, MN, NC, NJ, NY, OH, PA, TX, VA, and WI.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Alabama, Colorado, Florida, Georgia, Illinois, Maryland, Michigan, Minnesota, New Jersey, New York, North Carolina, Ohio, Pennsylvania, Texas, Virginia, Wisconsin.

Recall timeline

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

1. Firm started the recall: Nov 20, 202412. FDA classified it Class II: Dec 3, 202423. Published in FDA’s Enforcement Report: Dec 11, 202434. FDA terminated the recall: Apr 21, 2025420242025
  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 if I have this product?

Check the lot number on the jar. If it matches the affected lot numbers, you may want to stop using it if you are sensitive to artificial dyes.

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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-0252-2025 (November 20, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0252-2025 to see it in context.
  • Plain-language summary written by qwen3:4b on August 17, 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