CLASS I Food recall · Reported 12 Oct 2016 · FDA Enforcement Report

potato/whole peeled, Label states "Joe's Pride" recalled

Greenberg Fruit is recalling potato/whole peeled, Label states "Joe's Pride" and bears the address 9705 I Street, distributed in Nebraska. The recall was initiated on 15 Jul 2016 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot numbers: 160627, 16072, 16077, 16079, 160711, 160713, 160715
Quantity recalled58 cases (20 pounds each)

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-2613-2016
FDA event ID
74749
Recalling firm
Greenberg Fruit, Omaha, NE
Classification
Class I
Status
Terminated
Recall initiated
15 Jul 2016
FDA classified
30 Sep 2016
Reported
12 Oct 2016
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Listeria
Product category
Potatoes

Timeline

15 Jul 2016Recall initiated by company
30 Sep 2016Classified by FDA+77 days
12 Oct 2016Published 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

Routine environmental test samples were positive for Listeria monocytogenes on two processing machines.

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

potato/whole peeled, Label states "Joe's Pride" and bears the address 9705 I Street, Omaha, NE 68127. Product is packaged in poly bags inside cardboard boxes. All products have a best by date of 12 days after the production date.

Where it was distributed

Affected product was distributed to foodservice establishments in Omaha, Lincoln, and Bellevue, NE only.

Nebraska

Questions about this recall

Why was it recalled?

Routine environmental test samples were positive for Listeria monocytogenes on two processing machines.

Which lots are affected?

Lot numbers: 160627, 16072, 16077, 16079, 160711, 160713, 160715

Where was it sold?

Affected product was distributed to foodservice establishments in Omaha, Lincoln, and Bellevue, NE only.

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.

Other products in this recall event

9 other products · FDA event 74749

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