Warren Produce recalls Primo Fresh Serr: Salmonella risk in peppers
Warren Produce Co. recalls Primo Fresh Serrano Peppers due to Salmonella contamination. Consumers should avoid these products to prevent foodborne illness.
Lower-risk recall
Product tested positive for Salmonella
Contact the company
What happened, in plain English
Warren Produce is recalling Primo Fresh Serrano Peppers that tested positive for Salmonella. This poses a risk of foodborne illness if eaten, so affected consumers should avoid using these products. Read more at govinfonow.com/recall/23749-warren-produce-recalls-primo-fresh-serr-salmonella-risk-in-peppers.
Source Summary by GovInfoNow · govinfonow.com/recall/23749-warren-produce-recalls-primo-fresh-serr-salmonella-risk-in-peppers · Updated October 9, 2026 · FDA enforcement record: FDA #F-2036-2016
Cite this page
“Warren Produce recalls Primo Fresh Serr: Salmonella risk in peppers.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23749-warren-produce-recalls-primo-fresh-serr-salmonella-risk-in-peppers. Based on FDA recall #F-2036-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2036-2016%22&limit=1).
Why it’s dangerous
Salmonella bacteria can cause food poisoning, leading to symptoms like diarrhea, fever, and abdominal cramps. The product was found to contain Salmonella in testing, which can be harmful if consumed.
Who’s affected
Anyone who purchased Primo Fresh Serrano Peppers from Warren Produce in the U.S. between the specified dates. Children and elderly individuals are at higher risk for foodborne illness.
How to tell if you have this one
Check for Primo Fresh Serrano Peppers packaged in 1/4 bushel, 1 1/9 bushel, 10 lb, 5 lb, or 35 lb crates with the lot numbers 115158, 115181, or 115186.
- Brand
Warren Produce- Category
Food
What to do — step by step
Check Product Details
Look for the lot numbers 115158, 115181, or 115186 on the packaging of Primo Fresh Serrano Peppers.
Where it went and when
Where it was distributed
Distributed in 10 states.
FDA distribution: “TX, OK, KS, GA, CA, LA, IN, CO, MO, NY” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Colorado, Georgia, Indiana, Kansas, Louisiana, Missouri, New York, Oklahoma, Texas.
Recall timeline
FDA terminated this recall 5 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- 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-2036-2016 (July 22, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2036-2016 to see it in context.
- Plain-language summary written by qwen3:4b on October 9, 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.