Check the Batch
Class ITerminated in FDA datasetRecall initiated Oct 10, 2014

Mantequilla Hondurena (Honduran Style Butter Cream) in individually soft poly/plastic bags…

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.

ProductMantequilla Hondurena (Honduran Style Butter Cream) in individually soft poly/plastic bags labeled in part: Lacteos Santa Martha Mantequilla Hondurena Honduran Style Cream Net WT 1 LB (16 oz)
Package size1 LB
UPC635349000772

FDA code information

UPC 635349 000772 Best By dates: 07/01/14 thru 12/31/14

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Full FDA record and distribution details

Original product description

Mantequilla Hondurena (Honduran Style Butter Cream) in individually soft poly/plastic bags labeled in part: Lacteos Santa Martha Mantequilla Hondurena Honduran Style Cream Net WT 1 LB (16 oz)

Extracted codes and context

TypeCode / valueContext
UPC635349000772UPC 635349 000772 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-0605-2015
Event ID
69516
FDA status
Terminated
Initiated
Oct 10, 2014
Reported
Dec 10, 2014
Classified
Dec 2, 2014
Terminated
Mar 28, 2017
Quantity
2,371 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-0605-2015

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

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