Bolner's Fiesta Chili Pequino Recall: Low Peanuts Detected
Bolner's Fiesta recalls 0.25 oz Chili Pequino in clear plastic bags (Product Code 10106) due to low peanut contamination. Consumers should check product dates and contact for details.
Lower-risk recall
Low levels of peanuts detected
Contact the company
What happened, in plain English
Bolner's Fiesta is recalling 0.25 oz Chili Pequino products in clear plastic bags (Product Code 10106) because they contain low levels of peanuts. This recall affects people with peanut allergies who might react to the contamination. Read more at govinfonow.com/recall/20882-bolner-s-fiesta-chili-pequino-recall-low-peanuts-detected.
Source Summary by GovInfoNow · govinfonow.com/recall/20882-bolner-s-fiesta-chili-pequino-recall-low-peanuts-detected · Updated October 8, 2026 · FDA enforcement record: FDA #F-2385-2017
Cite this page
“Bolner's Fiesta Chili Pequino Recall: Low Peanuts Detected.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/20882-bolner-s-fiesta-chili-pequino-recall-low-peanuts-detected. Based on FDA recall #F-2385-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2385-2017%22&limit=1).
Why it’s dangerous
The chili peppers contain low levels of peanuts, which could trigger allergic reactions in sensitive individuals. This is a food safety issue for those with peanut allergies.
Who’s affected
People with peanut allergies who consume the recalled chili peppers may experience allergic reactions. The recall applies to specific packaging and dates.
How to tell if you have this one
Check for chili peppers in clear plastic bags labeled 'Chili Pequino 0.25 oz' with Product Code 10106. The product was sold between January 10, 2020, and April 10, 2020.
- Brand
Bolner's Fiesta- Category
Food
What to do — step by step
Check Product Details
Look for the product code 10106 on the packaging and verify the expiration date is between January 10, 2020, and April 10, 2020.
Where it went and when
Where it was distributed
Distributed in 20 states.
FDA distribution: “US. AR, AZ, CO, GA, ID, KS, LA, MI, MO, MS, MT, NE, NM, NV, OK, OR, TN, TX, UT, WY” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arizona, Arkansas, Colorado, Georgia, Idaho, Kansas, Louisiana, Michigan, Mississippi, Missouri, Montana, Nebraska, Nevada, New Mexico, Oklahoma, Oregon, Tennessee, Texas, Utah, Wyoming.
Recall timeline
FDA terminated this recall 3 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- 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-2385-2017 (June 12, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2385-2017 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.