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Lower risk Food recall · FDA · Published November 22, 2016

Coliman Pacific Jalapeno Peppers Recall: Salmonella Contamination Risk

Coliman Pacific Corp recalls jalapeno peppers due to potential Salmonella contamination. Consumers should check product labels for lot number 252414 to determine if affected.

🇺🇸 FDA recall #F-0768-2017FoodColiman Pacific ›
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Recalling firmColiman Pacific Corp4151 W Lindbergh Way · Chandler, AZ 85226-4719
✎ GovInfoNow plain-language explainer

What happened, in plain English

Coliman Pacific Corp is recalling jalapeno peppers that may be contaminated with Salmonella. This recall affects products sold in 40-pound cases with lot number 252414. Eating contaminated peppers could cause foodborne illness. Read more at govinfonow.com/recall/22824-coliman-pacific-jalapeno-peppers-recall-salmonella-contamination-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/22824-coliman-pacific-jalapeno-peppers-recall-salmonella-contamination-risk · Updated October 8, 2026 · FDA enforcement record: FDA #F-0768-2017

Cite this page

“Coliman Pacific Jalapeno Peppers Recall: Salmonella Contamination Risk.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/22824-coliman-pacific-jalapeno-peppers-recall-salmonella-contamination-risk. Based on FDA recall #F-0768-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0768-2017%22&limit=1).

Why it’s dangerous

Salmonella bacteria can cause food poisoning with symptoms like diarrhea, fever, and abdominal cramps. Contaminated peppers may be eaten without showing signs of illness initially, but can lead to serious health issues if not handled properly.

Who’s affected

Anyone who purchased or uses Coliman Pacific jalapeno peppers with lot number 252414. Children and elderly individuals are at higher risk for foodborne illness from Salmonella.

How to tell if you have this one

Check for lot number 252414 on the product label. The peppers are sold in 40-pound cases with a 1 1/9 Bushel Box packaging.

  • Brand
    Coliman Pacific
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for lot number 252414 on the packaging to confirm if your peppers are affected.

Where it went and when

Where it was distributed

Distributed in Arizona and California.

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: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: yesAZNew 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: “US: CA, AZ,” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Arizona, California.

Recall timeline

FDA terminated this recall 35 days after the firm started it.

1. Firm started the recall: Nov 22, 201612. FDA classified it Class I: Dec 19, 201623. FDA terminated the recall: Dec 27, 201634. Published in FDA’s Enforcement Report: Dec 28, 201642016
  1. Firm started the recall
  2. FDA classified it Class I
  3. FDA terminated the recall
  4. Published in FDA’s Enforcement Report

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-0768-2017 (November 22, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0768-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 8, 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