Crema Cuzcatlan (Salvadorean Style Cream) in individually soft poly/plastic bags labeled in part: Lacteos Santa Martha Crema Cuzcatlan Salvadorean Style Cream Net WT 1 LB (16 oz)
Class I - DangerousWhat Should You Do?
- Check if you have this product: UPC 635349 000444 Best By dates: 07/01/14 thru 12/31/14
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- 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:
Crema Cuzcatlan (Salvadorean Style Cream) in individually soft poly/plastic bags labeled in part: Lacteos Santa Martha Crema Cuzcatlan Salvadorean Style Cream Net WT 1 LB (16 oz)
Product Codes/Lot Numbers:
UPC 635349 000444 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.govFDA Recall Number: F-0610-2015
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