Deli-Food Ancho Chile Powder Recalled for Salmonella Risk
Deli-Food Chili & Spice LLC recalls 2,250 lbs of Ancho Chile Powder due to Salmonella contamination. Check your lot number C-01772-16069.
Stop using this now
Deli-Food Chili & Spice LLC announces a voluntary field action for Ancho Chile Powder due to positive testing for Salmonella.
Contact the company
What happened, in plain English
Deli-Food Chili & Spice LLC is recalling 2,250 pounds of Ancho Chile Powder because it tested positive for Salmonella. The product was sold in 50 lb corrugated boxes to consignees in Maryland and Ohio. No specific remedy or return instructions are provided in the record. Read more at govinfonow.com/recall/24035-deli-food-ancho-chile-powder-recalled-for-salmonella-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/24035-deli-food-ancho-chile-powder-recalled-for-salmonella-risk · Updated October 9, 2026 · FDA enforcement record: FDA #F-1872-2016
Cite this page
“Deli-Food Ancho Chile Powder Recalled for Salmonella Risk.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/24035-deli-food-ancho-chile-powder-recalled-for-salmonella-risk. Based on FDA recall #F-1872-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1872-2016%22&limit=1).
Why it’s dangerous
The powder is contaminated with Salmonella, a bacterium that can cause serious foodborne illness. Ingesting the product poses a health risk to anyone who consumes it.
Who’s affected
Commercial buyers or food service establishments in Maryland and Ohio who purchased these 50 lb boxes of Ancho Chile Powder. Consumers should be cautious if they acquired this product through a commercial distributor.
How to tell if you have this one
Look for Ancho Chile Powder in 50 lb corrugated boxes. The specific lot number to check is C-01772-16069. The product was distributed to two consignees in Maryland and Ohio.
- Brand
Deli-Food- Category
Food
What to do — step by step
Stop Using the Product
Do not use or distribute the Ancho Chile Powder due to Salmonella contamination.
Check Lot Number
Verify if your product matches lot number C-01772-16069.
Where it went and when
Where it was distributed
Distributed in Maryland and Ohio.
FDA distribution: “2 consignees in Maryland and Ohio. No Canadian/foreign/VA/govt/military.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Maryland, Ohio.
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-1872-2016 (June 10, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1872-2016 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b 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.