CLASS I Food recall · Reported 28 Sep 2016 · FDA Enforcement Report

Sweet Pea Pasta Salad cardboard case (2) rigid Keep Refrigerated recalled

Dutch Treat Salads is recalling Sweet Pea Pasta Salad cardboard case (2) rigid Keep Refrigerated, distributed in Michigan. The recall was initiated on 17 Jun 2016 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesUse by dates through July 1, 2016
Quantity recalled3107 lbs

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-2357-2016
FDA event ID
74476
Recalling firm
Dutch Treat Salads, Zeeland, MI
Classification
Class I
Status
Terminated
Recall initiated
17 Jun 2016
FDA classified
16 Sep 2016
Reported
28 Sep 2016
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Listeria
Product category
Salad Kits

Timeline

17 Jun 2016Recall initiated by company
16 Sep 2016Classified by FDA+91 days
28 Sep 2016Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Product has potential of being contaminated with Listeria monocytogenes.

Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.

Product as listed by the FDA

Sweet Pea Pasta Salad 10 lb cardboard case (2, 5lb plastic bags), 2 lb rigid plastic container, 14 oz. rigid plastic container Keep Refrigerated

Where it was distributed

MI only

Michigan

Questions about this recall

Why was it recalled?

Product has potential of being contaminated with Listeria monocytogenes.

Which lots are affected?

Use by dates through July 1, 2016

Where was it sold?

MI only

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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