CLASS II Food recall · Reported 7 Nov 2012 · FDA Enforcement Report

"***Productos El Gauchito Empanadillas Argentinas de Queso recalled

Productos El Gauchito is recalling "***Productos El Gauchito Empanadillas Argentinas de Queso y Cebolla (Cheese and, distributed in Puerto Rico. The recall was initiated on 20 Aug 2012 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesNo code or lot numbers.
Quantity recalledN/A

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-0568-2013
FDA event ID
62923
Recalling firm
Productos El Gauchito, Bayamon, PR
Classification
Class II
Status
Terminated
Recall initiated
20 Aug 2012
FDA classified
31 Oct 2012
Reported
7 Nov 2012
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Undeclared Soy
Product category
Cheese

Timeline

20 Aug 2012Recall initiated by company
31 Oct 2012Classified by FDA+72 days
7 Nov 2012Published in enforcement report+7 days

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

Reason for recall

Undeclared soy, FD&C Yellow #6 and Red #40 contained in soft dough shells.

Product as listed by the FDA

"***Productos El Gauchito Empanadillas Argentinas de Queso y Cebolla (Cheese and OnionTurnovers)***keep frozen or refrigerated***consumer contact: [email protected] Av. Minillas NM-16 Bayamon PR 00956***"

Where it was distributed

Puerto Rico only (hotels, gas stations, restaurants)

Puerto Rico

Questions about this recall

Why was it recalled?

Undeclared soy, FD&C Yellow #6 and Red #40 contained in soft dough shells.

Which lots are affected?

No code or lot numbers.

Where was it sold?

Puerto Rico only (hotels, gas stations, restaurants)

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.

Other products in this recall event

3 other products · FDA event 62923

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