FDA recall record

Oasis Brands Queso Seco Centroamericano recall — FDA F-0595-2015

Virginia State (VDACS) found Listeria monocytogenes in Lacteos Santa Martha Quesito Casero Fresh Curd; FDA made an inspection, were the environmental…

Class Iclassification
F-0595-2015official record ID
Dec 10, 2014report date

Recall record at a glance

Official recordF-0595-2015
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmOasis Brands, Inc.
Report dateDec 10, 2014
Recall initiation dateOct 10, 2014
Quantity1,921 pieces
LocationMiami, FL, United States

Official product description

Queso Seco Centroamericano (Cheese) in individually soft poly/plastic bags labeled in part: Lacteos Santa Martha Queso Seco Centroamericano Dry White Cheese Net Wt 1LB (16oz)

Why the product was recalled

Virginia State (VDACS) found Listeria monocytogenes in Lacteos Santa Martha Quesito Casero Fresh Curd; FDA made an inspection, were the environmental samples that came up positive also for Listeria monocytogenes, also the firm sent samples to a private lab that came positive for Listeria monocytogenes in various products. The firm is voluntarily recalling all their Lacteos Santa Martha products manufactured that are within expiration date.

Distribution information

FL, GA. NC, and TN

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

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