CLASS I Food recall · Reported 12 Apr 2017 · FDA Enforcement Report

artisanal cheese Vulto Creamery Handmade Cheese, Walton Umber recalled

Vulto Creamery is recalling artisanal cheese Vulto Creamery Handmade Cheese, Walton Umber, distributed nationwide in the US. The recall was initiated on 3 Mar 2017 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesall lots
Quantity recalled484 wheels

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-1859-2017
FDA event ID
76649
Recalling firm
Vulto Creamery, Walton, NY
Classification
Class I
Status
Terminated
Recall initiated
3 Mar 2017
FDA classified
4 Apr 2017
Reported
12 Apr 2017
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Listeria
Product category
Cheese

Timeline

3 Mar 2017Recall initiated by company
4 Apr 2017Classified by FDA+32 days
12 Apr 2017Published in enforcement report+8 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

artisanal cheese VULTO Creamery HANDMADE CHEESE, Walton Umber, NET WT. 4 lbs

Where it was distributed

Nationwide with most being sold at retail locations in the Northeastern and Mid-Atlantic States, California, Chicago IL, Portland Oregon and Washington, DC.

Nationwide CaliforniaDistrict of ColumbiaIllinoisOregonWashington

Questions about this recall

Is artisanal cheese Vulto Creamery Handmade Cheese, Walton Umber recalled?

Yes. Vulto Creamery recalled artisanal cheese Vulto Creamery Handmade Cheese, Walton Umber on 3 Mar 2017. The recall is Class I and its status is Terminated. Recall number F-1859-2017.

Why was it recalled?

Listeria monocytogenes contamination

Which lots are affected?

all lots

Where was it sold?

Nationwide with most being sold at retail locations in the Northeastern and Mid-Atlantic States, California, Chicago IL, Portland Oregon and Washington, DC.

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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