CLASS I Food recall · Reported 11 Nov 2015 · FDA Enforcement Report

Organic Roquefort Papillon cheese recalled by Whole Foods Market

Whole Foods Market is recalling Organic Roquefort Papillon cheese, distributed nationwide in the US. The recall was initiated on 7 Oct 2015 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesPLU 029536, all sell by dates
Quantity recalled1593 pounds

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-0130-2016
FDA event ID
72370
Recalling firm
Whole Foods Market, Austin, TX
Classification
Class I
Status
Terminated
Recall initiated
7 Oct 2015
FDA classified
5 Nov 2015
Reported
11 Nov 2015
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Listeria
Product category
Ready Meals

Timeline

7 Oct 2015Recall initiated by company
5 Nov 2015Classified by FDA+29 days
11 Nov 2015Published 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

Potential contamination 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

Organic Roquefort Papillon cheese packaged in clear plastic wrap

Where it was distributed

Nationwide throughout the USA and UK

Nationwide

Stores named: Whole Foods

Questions about this recall

Why was it recalled?

Potential contamination with Listeria monocytogenes.

Which lots are affected?

PLU 029536, all sell by dates

Where was it sold?

Nationwide throughout the USA and UK

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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