Crema Cuzcatlan
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…
Lacteos Santa Martha Quesito Casero Fresh Curd recall
Recalled by Oasis Brands, Inc · Miami, FL, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
A State sample came positive for Listeria monocytogenes
Pathogen: Listeria
Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
Lacteos Santa Martha Quesito Casero Fresh Curd Net Weight 12oz Distributed by Oasis Brands Inc., Miami FL 33192
Quantity: 375 units
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
UPC 635349 000420 / Exp. Date 092714
Where it was sold
Georgia North Carolina South Carolina Tennessee Virginia
FDA's distribution note: NC (Further shipment by the NC distributors is: TN, VA, NC, SC, and GA).
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Oasis Brands, Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jul 31, 2014
- In FDA report of
- Sep 10, 2014
- Terminated
- Mar 28, 2017
- FDA recall number
- F-2060-2014 · event 68958
- Official record
- FDA enforcement report search
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