Spicely Organics Tarragon Recall: Potential Salmonella Risk
Spicely Organics recalls 0.4oz organic tarragon due to potential Salmonella contamination. Check UPC 826998041067 for affected products.
Lower-risk recall
Potential Salmonella contamination.
Contact the company
What happened, in plain English
Spicely Organics is recalling organic tarragon that may contain Salmonella. This could cause food poisoning if eaten. Consumers should check the UPC code to see if they have the affected product. Read more at govinfonow.com/recall/20376-spicely-organics-tarragon-recall-potential-salmonella-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/20376-spicely-organics-tarragon-recall-potential-salmonella-risk · Updated October 7, 2026 · FDA enforcement record: FDA #F-0131-2018
Cite this page
“Spicely Organics Tarragon Recall: Potential Salmonella Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/20376-spicely-organics-tarragon-recall-potential-salmonella-risk. Based on FDA recall #F-0131-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0131-2018%22&limit=1).
Why it’s dangerous
Salmonella is a bacteria that can cause food poisoning. If the tarragon is contaminated, eating it could lead to symptoms like diarrhea, fever, and stomach cramps.
Who’s affected
Anyone who purchased Spicely Organics Organic Tarragon 0.4oz (11g) with UPC 826998041067 from 2020. People with compromised immune systems are at slightly higher risk.
How to tell if you have this one
Check for UPC code 826998041067 on the product label. The product was sold with lot number OTW100134 and best by date 12/31/2020.
- Brand
Spicely Organics- Product
Spicely Organics Organic Tarragon 0.4oz. (11g) UPC codes: 8 26998 04106 7- Category
Food
What to do — step by step
Check Product UPC
Look for UPC code 826998041067 on the tarragon packaging.
Where it went and when
Where it was distributed
Distributed in 21 states.
FDA distribution: “U.S. distribution to the following: Alaska, Arizona, California, Colorado, Hawaii, Illinois, Indiana, Kansas, Maryland, Michigan, Minnesota, Nevada, New Mexico, New York, Ohio, Oregon, Pennsylvania, Texas, Virginia, Washington and…” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Alaska, Arizona, California, Colorado, Hawaii, Illinois, Indiana, Kansas, Maryland, Michigan, Minnesota, Nevada, New Mexico, New York, Ohio, Oregon, Pennsylvania, Texas, Virginia, Washington, Wisconsin.
Recall timeline
FDA terminated this recall 3 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-0131-2018 (October 9, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0131-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 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.