CLASS I Food recall · Reported 1 Mar 2017 · FDA Enforcement Report

Soureliette cheese recalled by Fromi Usa Corp C/o Natixis

Fromi Usa Corp C/o Natixis Prame is recalling Soureliette cheese, distributed in California, Massachusetts, New York. The recall was initiated on 21 Dec 2016 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesProduct Number Art.-Nr. 707116 MHD, 22.01.2017, MHD 08.02.2017, MHD 22.02.2017
Quantity recalled7 cases/3.969 lb/1.323 lb per unit

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-1533-2017
FDA event ID
76366
Recalling firm
Fromi Usa Corp C/o Natixis Prame, New York, NY
Classification
Class I
Status
Terminated
Recall initiated
21 Dec 2016
FDA classified
23 Feb 2017
Reported
1 Mar 2017
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Listeria
Product category
Cheese

Timeline

21 Dec 2016Recall initiated by company
23 Feb 2017Classified by FDA+64 days
1 Mar 2017Published in enforcement report+6 days

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

Reason for recall

Listeria monocytogenes contamination

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

Soureliette cheese, Net Wt 3.969 lb (case)/ Net Wt 1.323 lb per unit, Item number 707116

Where it was distributed

CA, NY & MA thru four retail stores

CaliforniaMassachusettsNew York

Questions about this recall

Is Soureliette cheese recalled?

Yes. Fromi Usa Corp C/o Natixis Prame recalled Soureliette cheese on 21 Dec 2016. The recall is Class I and its status is Terminated. Recall number F-1533-2017.

Why was it recalled?

Listeria monocytogenes contamination

Which lots are affected?

Product Number Art.-Nr. 707116 MHD, 22.01.2017, MHD 08.02.2017, MHD 22.02.2017

Where was it sold?

CA, NY & MA thru four retail stores

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 21 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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