Arro 10.0 Grams Chili Spice Blend Recall: Possible Salmonella Contamination
Arro Corporation recalls 10.0 Grams Chili Spice Blend packets with possible Salmonella contamination. Consumers should check lot numbers 5389705300AA and 53897:150
Recall notice
Possible contamination of chili seasoning mix with Salmonella.
Contact the company
What happened, in plain English
Arro Corporation is recalling 10.0 Grams Chili Spice Blend packets due to possible Salmonella contamination. This could cause foodborne illness if consumed. Read more at govinfonow.com/recall/21909-arro-10-0-grams-chili-spice-blend-recall-possible-salmonella.
Source Summary by GovInfoNow · govinfonow.com/recall/21909-arro-10-0-grams-chili-spice-blend-recall-possible-salmonella · Updated October 8, 2026 · FDA enforcement record: FDA #F-2141-2017
Cite this page
“Arro 10.0 Grams Chili Spice Blend Recall: Possible Salmonella Contamination.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/21909-arro-10-0-grams-chili-spice-blend-recall-possible-salmonella. Based on FDA recall #F-2141-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2141-2017%22&limit=1).
Why it’s dangerous
Salmonella is a bacteria that can cause food poisoning. If the chili spice blend is contaminated with Salmonella, eating it could lead to illness.
Who’s affected
Anyone who owns or uses the recalled 10.0 Grams Chili Spice Blend packets. People who have consumed the product are at risk of foodborne illness.
How to tell if you have this one
Check for lot numbers 5389705300AA and 5389705400AA on the product packaging. The product is sold in 10.0 Gram packets.
- Brand
Arro Corporation- Category
Food
What to do — step by step
Check Product Lot Number
Look for lot numbers 5389705300AA or 5389705400AA on the product packaging.
Where it went and when
Where it was distributed
Distributed in Ohio.
FDA distribution: “OH” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Ohio.
Recall timeline
FDA terminated this recall 2.1 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-2141-2017 (March 29, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2141-2017 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.