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Class ITerminated in FDA datasetRecall initiated Oct 10, 2014

Crema Centroamericana (Centroamerican Style Soft Blend Dairy Spread) in individually soft…

Recalling firm: Oasis Brands, Inc

Why it was recalled

Virginia State (VDACS) found Listeria monocytogenes in Lacteos Santa Martha Quesito Casero Fresh Curd (Best by 9/27/14), FDA made an inspection, were the environmental samples…

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Mar 28, 2017.

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Compare the exact product and package details with the label you have.

ProductCrema Centroamericana (Centroamerican Style Soft Blend Dairy Spread) in individually soft poly/plastic bags labeled in part: Lacteos Santa Martha Crema Centroamericana Net Wt 1LB (16oz)
Package size1LB
UPC876593001898

FDA code information

UPC 876593 001898 Best By dates: 07/01/14 thru 12/31/14

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Full FDA record and distribution details

Original product description

Crema Centroamericana (Centroamerican Style Soft Blend Dairy Spread) in individually soft poly/plastic bags labeled in part: Lacteos Santa Martha Crema Centroamericana Net Wt 1LB (16oz)

Extracted codes and context

TypeCode / valueContext
UPC876593001898UPC 876593 001898 Best By dates: 07/01/14 thru 12/31/14

Original FDA recall reason

Virginia State (VDACS) found Listeria monocytogenes in Lacteos Santa Martha Quesito Casero Fresh Curd (Best by 9/27/14), FDA made an inspection, were the environmental samples collected came up positive also for Listeria monocytogenes, also the Oasis Brands Inc. sent finish products samples to a private lab, the Lacteos Santa Martha Cuajada en Hoja Queso Casero Hecho a Mano Fresh Curd (Best By dates of 10/18/14 and 11/25/14) came also positive for Listeria monocytogenes. Oasis Brands Inc. is voluntarily recalling ALL their Lacteos Santa Martha brand products manufactured that are within expiration date.

Recall details

Recall number
F-0604-2015
Event ID
69516
FDA status
Terminated
Initiated
Oct 10, 2014
Reported
Dec 10, 2014
Classified
Dec 2, 2014
Terminated
Mar 28, 2017
Quantity
6,369 pieces
Location
Miami, FL, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

FL, GA. NC, and TN

FDA source record · F-0604-2015

Data updated September 16, 2026. View official FDA data ↗

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