ChloroFields Micro-greens Asian Mix Recall: Salmonella Contamination Risk
ChloroFields recalls 1.5 oz Asian mix greens potentially contaminated with Salmonella. Consumers should check product codes and take action if affected.
Lower-risk recall
Salad greens potentially contaminated with Salmonella
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What happened, in plain English
ChloroFields is recalling its Micro-greens Asian Mix due to potential Salmonella contamination. This poses a health risk if consumed, as Salmonella can cause foodborne illness. Read more at govinfonow.com/recall/21939-chlorofields-micro-greens-asian-mix-recall-salmonella-contamination-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/21939-chlorofields-micro-greens-asian-mix-recall-salmonella-contamination-risk · Updated October 8, 2026 · FDA enforcement record: FDA #F-1988-2017
Cite this page
“ChloroFields Micro-greens Asian Mix Recall: Salmonella Contamination Risk.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/21939-chlorofields-micro-greens-asian-mix-recall-salmonella-contamination-risk. Based on FDA recall #F-1988-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1988-2017%22&limit=1).
Why it’s dangerous
Salmonella bacteria can cause food poisoning with symptoms like diarrhea, fever, and abdominal cramps. The contamination occurred during production, making the greens unsafe to eat.
Who’s affected
Anyone who purchased ChloroFields Micro-greens Asian Mix (1.5 oz, clear plastic clamshells) between March 2017 and the sell-by date. Young children and elderly individuals are at higher risk for foodborne illness.
How to tell if you have this one
Check for the product code H03082014A116C117BR118R119MB120L121 on the packaging. The product was sold with a sell-by date of March 26, 2017.
- Brand
ChloroFields- Category
Food
What to do — step by step
Check Product Code
Look for the product code H03082014A116C117BR118R119MB120L121 on the packaging.
Where it went and when
Where it was distributed
Distributed in Colorado and Kansas.
FDA distribution: “Product distribute to the following US States: Kansas and Colorado.” 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 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-1988-2017 (March 22, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1988-2017 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.