CLASS II Food recall · Reported 5 Apr 2017 · FDA Enforcement Report

La Fe Papa Criollas Yellow Potato recalled by Grace Kennedy Foods USA

Grace Kennedy Foods USA is recalling La Fe Papa Criollas Yellow Potato, distributed nationwide in the US. The recall was initiated on 20 Feb 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codeslote 225 16 vence 12 08 18
Quantity recalled2005 cases

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-1808-2017
FDA event ID
76550
Recalling firm
Grace Kennedy Foods USA, Moonachie, NJ
Brand
La Fe
Classification
Class II
Status
Terminated
Recall initiated
20 Feb 2017
FDA classified
30 Mar 2017
Reported
5 Apr 2017
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Listeria
Product category
Potatoes

Timeline

20 Feb 2017Recall initiated by company
30 Mar 2017Classified by FDA+38 days
5 Apr 2017Published 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

La Fe Papas Criollos may be contaminated with Listeria Monoctyogenes.

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

La Fe Papa Criollas Yellow Potato Net Wt. 14 oz. Distributed: by La Fe Foods Moonachne, NJ 07074 UPC

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Why was it recalled?

La Fe Papas Criollos may be contaminated with Listeria Monoctyogenes.

Which lots are affected?

lote 225 16 vence 12 08 18

Where was it sold?

Nationwide

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

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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