Dutch Treat Sweet Pea Pasta Salad Recalled for Listeria Risk
Dutch Treat Salads Inc. recalls Sweet Pea Pasta Salad due to potential Listeria monocytogenes contamination. Check your fridge for affected lots.
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Product has potential of being contaminated with Listeria monocytogenes.
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What happened, in plain English
Dutch Treat Salads Inc. is recalling Sweet Pea Pasta Salad because it may be contaminated with Listeria monocytogenes. This bacteria can cause serious illness, particularly for vulnerable populations. The recall covers products distributed in Michigan with use-by dates through July 1, 2016. Read more at govinfonow.com/recall/23948-dutch-treat-sweet-pea-pasta-salad-recalled-for-listeria-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/23948-dutch-treat-sweet-pea-pasta-salad-recalled-for-listeria-risk · Updated October 9, 2026 · FDA enforcement record: FDA #F-2357-2016
Cite this page
“Dutch Treat Sweet Pea Pasta Salad Recalled for Listeria Risk.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23948-dutch-treat-sweet-pea-pasta-salad-recalled-for-listeria-risk. Based on FDA recall #F-2357-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2357-2016%22&limit=1).
Why it’s dangerous
Listeria monocytogenes is a bacteria that can cause serious infections in humans. Ingestion of contaminated food can lead to severe illness, especially for high-risk groups.
Who’s affected
Consumers in Michigan who purchased Sweet Pea Pasta Salad with use-by dates through July 1, 2016. Individuals at higher risk for Listeria infection, such as pregnant women, older adults, and those with weakened immune systems, are most at risk.
How to tell if you have this one
Check for Sweet Pea Pasta Salad sold by Dutch Treat Salads Inc. Look for packaging in 10 lb cardboard cases (containing two 5lb plastic bags), 2 lb rigid plastic containers, or 14 oz rigid plastic containers. Verify the use-by date is through July 1, 2016.
- Brand
Dutch Treat Salads- Category
Food
Where it went and when
Where it was distributed
Distributed in Michigan.
FDA distribution: “MI only” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Michigan.
Recall timeline
FDA terminated this recall 9 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-2357-2016 (June 17, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2357-2016 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b 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.