CLASS I Food recall · Reported 5 Sep 2012 · FDA Enforcement Report

Whole Fresh Cantaloupe recalled by Burch Farms

Burch Farms is recalling Whole Fresh Cantaloupe, distributed in 10 states. The recall was initiated on 28 Jul 2012 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesPLU 4319
Quantity recalled580 cases (9 whole cantaloupes per case). Additional188,902 cantaloupes.

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-2031-2012
FDA event ID
62687
Recalling firm
Burch Farms, Faison, NC
Classification
Class I
Status
Terminated
Recall initiated
28 Jul 2012
FDA classified
24 Aug 2012
Reported
5 Sep 2012
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Listeria
Product category
Strawberries

Timeline

28 Jul 2012Recall initiated by company
24 Aug 2012Classified by FDA+27 days
5 Sep 2012Published 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 was found to be 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

Whole Fresh Cantaloupe, PLU# 4319, Burch Farms, Faison, NC 28341. On 8/2/2012 the recall was expanded to include cantaloupes labeled, Cottle Strawberry, Inc., #4319, Faison, NC. (Cottle Farms is not involved in this recall).

Where it was distributed

NY; Expanded on 8/2 to include FL, GA, IL, MD, NC, NJ, PA, SC and VA.

FloridaGeorgiaIllinoisMarylandNorth CarolinaNew JerseyNew YorkPennsylvaniaSouth CarolinaVirginia

Questions about this recall

Is Whole Fresh Cantaloupe recalled?

Yes. Burch Farms recalled Whole Fresh Cantaloupe on 28 Jul 2012. The recall is Class I and its status is Terminated. Recall number F-2031-2012.

Why was it recalled?

Product was found to be contaminated with Listeria monocytogenes.

Which lots are affected?

PLU 4319

Where was it sold?

NY; Expanded on 8/2 to include FL, GA, IL, MD, NC, NJ, PA, SC and VA.

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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