Osage Gardens Organic Micro Greens Recall: Salmonella Risk
Osage Gardens recalls Organic 2oz Micro Greens with Salmonella contamination. Keep refrigerated; Julian codes 266, 269, 272, 274, 279.
Lower-risk recall
Osage Gardens announces a voluntary recall of Organic 2oz Micro Greens due to a positive test for Salmonella.
Contact the company
What happened, in plain English
Osage Gardens is recalling Organic 2oz Micro Greens due to Salmonella contamination. This poses a risk of foodborne illness, especially for vulnerable groups like young children, elderly, or those with weakened immune systems. Read more at govinfonow.com/recall/23061-osage-gardens-organic-micro-greens-recall-salmonella-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/23061-osage-gardens-organic-micro-greens-recall-salmonella-risk · Updated October 9, 2026 · FDA enforcement record: FDA #F-0375-2017
Cite this page
“Osage Gardens Organic Micro Greens Recall: Salmonella Risk.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23061-osage-gardens-organic-micro-greens-recall-salmonella-risk. Based on FDA recall #F-0375-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0375-2017%22&limit=1).
Why it’s dangerous
Salmonella is a bacteria that can cause food poisoning, leading to symptoms like diarrhea, fever, and abdominal cramps. While usually not life-threatening, it can be serious for vulnerable populations.
Who’s affected
People who purchased Organic 2oz Micro Greens from Osage Gardens with Julian codes 266, 269, 272, 274, or 279. Those most at risk include young children, elderly individuals, and people with compromised immune systems.
How to tell if you have this one
Check for Organic 2oz Micro Greens in clear plastic clamshells with Julian codes 266, 269, 272, 274, or 279. The product must be kept refrigerated as per the label.
- Brand
Osage Gardens- Category
Food
What to do — step by step
Check Product Codes
Look for Julian codes 266, 269, 272, 274, or 279 on the product label.
Where it went and when
Where it was distributed
Distributed in Colorado and Kansas, and outside the U.S.
FDA distribution: “Colorado and Kansas. No Canadian, VA/govt/military or other foreign consignees.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Colorado, Kansas.
Recall timeline
FDA terminated this recall 2 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-0375-2017 (October 7, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0375-2017 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.