🔍 RecallPedia

My Queso (Latin Flavor Cheese) in individually soft poly/plastic bags labeled in part: Lacteos Santa Martha My Queso Latin Flavor Cheese Net Wt 1LB (16oz)

Class I - Dangerous
Recalled: October 10, 2014 Oasis Brands Dairy & Eggs

What Should You Do?

  1. Check if you have this product:
    UPC 635349 000406 Best By dates: 07/01/14 thru 12/31/14
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Oasis Brands, Inc
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.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

My Queso (Latin Flavor Cheese) in individually soft poly/plastic bags labeled in part: Lacteos Santa Martha My Queso Latin Flavor Cheese Net Wt 1LB (16oz)

Product Codes/Lot Numbers:

UPC 635349 000406 Best By dates: 07/01/14 thru 12/31/14

Distribution:

Distributed in: FL, GA, NC, TN

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0599-2015

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