CLASS I Food recall · Reported 4 Sep 2013 · FDA Enforcement Report

Cilantro, fresh bunch, #4889 recalled by Buurma Farms

Buurma Farms is recalling Cilantro, fresh bunch, #4889, distributed in Illinois, Indiana, Michigan, Ohio. The recall was initiated on 15 Aug 2013 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot # 02D312A4
Quantity recalled468 boxes

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-1852-2013
FDA event ID
66023
Recalling firm
Buurma Farms, Willard, OH
Classification
Class I
Status
Terminated
Recall initiated
15 Aug 2013
FDA classified
26 Aug 2013
Reported
4 Sep 2013
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Listeria
Product category
Fresh Herbs

Timeline

15 Aug 2013Recall initiated by company
26 Aug 2013Classified by FDA+11 days
4 Sep 2013Published in enforcement report+9 days

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

Reason for recall

The firm was notified by one of their customers of a positive Listeria monocytogenes results they received from the Michigan Department of Agriculture.

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

Buurma Farms Cilantro, fresh, 4 oz bunch, #4889 UPC 0 33383 80104 9

Where it was distributed

Product was distributed to the following states: IL, IN, MI and OH.

IllinoisIndianaMichiganOhio

Questions about this recall

Why was it recalled?

The firm was notified by one of their customers of a positive Listeria monocytogenes results they received from the Michigan Department of Agriculture.

Which lots are affected?

Lot # 02D312A4

Where was it sold?

Product was distributed to the following states: IL, IN, MI and OH.

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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