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Class I: serious health riskTerminated

Oasis Brands Cuajada en Hoja Recall

Cuajada en Hoja (Fresh Curd Cheese) in individually soft poly/plastic bags labeled in p…

Oasis Brands, Inc · Miami, FL

Risk level
Class I
Reported by FDA
Dec 10, 2014
Recall ID
F-0603-2015
Check your lot numberHow we source this data

Summary

Oasis Brands recalled Cuajada en Hoja starting Oct 10, 2014. The FDA classified it as Class I (serious health risk) and published enforcement report F-0603-2015 on Dec 10, 2014. 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. Status: Terminated.

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 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.

Product description

Cuajada en Hoja (Fresh Curd Cheese) in individually soft poly/plastic bags labeled in part: Lacteos Santa Martha Cuajada en Hoja Queso Casero Hecho a Mano Fresh Curd Net Wt 12oz (340g)

Lot numbers, UPCs & expiration codes

UPC 635349 000895 Best By dates: 07/01/14 thru 12/31/14

Where it was sold

FL, GA. NC, and TN

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-0603-2015
Classification
Class I
Status
Terminated
Recall initiated
Oct 10, 2014
FDA report date
Dec 10, 2014
Quantity
37,126 pieces
Recall type
Voluntary: Firm initiated
Recalling firm
Oasis Brands, Inc

Original FDA data

Every field from FDA enforcement report F-0603-2015, exactly as published.

Show all FDA fields
City
Miami
State
FL
Status
Terminated
Country
United States
Event ID
69516
Address
13439 NW 19 LANE
Code information
UPC 635349 000895 Best By dates: 07/01/14 thru 12/31/14
Postal code
33182
Report date
Dec 10, 2014
Product type
Food
Recall number
F-0603-2015
Classification
Class I
Recalling firm
Oasis Brands, Inc
Product quantity
37,126 pieces
Termination date
Mar 28, 2017
Reason for recall
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.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Cuajada en Hoja (Fresh Curd Cheese) in individually soft poly/plastic bags labeled in part: Lacteos Santa Martha Cuajada en Hoja Queso Casero Hecho a Mano Fresh Curd Net Wt 12oz (340g)
Distribution pattern
FL, GA. NC, and TN
Recall initiation date
Oct 10, 2014
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Dec 2, 2014

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0603-2015, published Dec 10, 2014. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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