ConAgra Premium Hunt's Chili Kit Recall: Salmonella Risk in Spice Packets
ConAgra recalls Premium Hunt's Chili Kits with potential Salmonella contamination in spice packets. Consumers should check lot numbers and follow safety steps to avoid foodborne illness.
Lower-risk recall
Potential Salmonella contamination of spice packet within chili kits.
Contact the company
What happened, in plain English
ConAgra is recalling Premium Hunt's Chili Kits that may contain Salmonella in the spice packets. This could cause food poisoning if the contaminated spice is eaten. Read more at govinfonow.com/recall/21900-conagra-premium-hunt-s-chili-kit-recall-salmonella-risk-in.
Source Summary by GovInfoNow · govinfonow.com/recall/21900-conagra-premium-hunt-s-chili-kit-recall-salmonella-risk-in · Updated October 8, 2026 · FDA enforcement record: FDA #F-2095-2017
Cite this page
“ConAgra Premium Hunt's Chili Kit Recall: Salmonella Risk in Spice Packets.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/21900-conagra-premium-hunt-s-chili-kit-recall-salmonella-risk-in. Based on FDA recall #F-2095-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2095-2017%22&limit=1).
Why it’s dangerous
The spice packet inside the chili kit may contain Salmonella bacteria, which can cause food poisoning if eaten. This happens because the spice packet is not properly sealed during manufacturing, allowing bacteria to grow.
Who’s affected
Anyone who purchased the recalled Premium Hunt's Chili Kits with lot numbers 3534619500, 3534622200, or 3534619600. People who have already cooked the chili with the contaminated spice packet are at higher risk.
How to tell if you have this one
Check the product label for lot numbers 3534619500, 3534622200, or 3534619600. The product is sold in 44.8 oz (2.80 lb) packages with directions for cooking.
- Brand
ConAgra- Category
Food
What to do — step by step
Check Product Lot Number
Look for lot numbers 3534619500, 3534622200, or 3534619600 on the package.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 2.2 years 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-2095-2017 (March 31, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2095-2017 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.