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WASHINGTON, November 22, 2013 – DelMonaco Specialty Foods, a Morgan Hill, Calif. establishment, is recalling approximately 5,616 pounds of Armanino brand Bolognese sauce products because of an undeclared allergen and misbranding, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today. The product contains milk, a known allergen which was declared on the product label; however the label was not applied to all the products in each lot.
The Bolognese Sauce with Beef & Pork products were produced on September 25, September 27, and November 7, 2013. The following products are subject to recall:
The problem was discovered by the company’s customer. FSIS and the company have received no reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a health care provider.
FSIS routinely conducts recall effectiveness checks to verify that recalling firms notify theircustomers of the recall and that steps are taken to make certain that the product is no longer available to consumers.
Media outlets with questions regarding the recall can contact Arnold Avalos, VP of Operations, at 408-500-4118. Consumers with questions regarding the recall can contact Sandra Johnson, Sales Coordinator, at 408-500-4114.
The Bolognese Sauce with Beef & Pork products were produced on September 25, September 27, and November 7, 2013. The following products are subject to recall:
- 7.5 pound cases containing twelve 10-ounce bags of “Bolognese Sauce with Beef & Pork” with case number 31113 printed on the interior bag.
- 7.5 pound cases containing twelve 10-ounce bags of “Bolognese Sauce with Beef & Pork” with case number 27013 printed on the interior bag.
- 12 pound cases containing four 3-pound bags of “Bolognese Sauce with Beef & Pork” with case number 31113 printed on the interior bag.
- 12 pound cases containing four 3-pound bags of “Bolognese Sauce with Beef & Pork” with case number 26813 printed on the interior bag.
The problem was discovered by the company’s customer. FSIS and the company have received no reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a health care provider.
FSIS routinely conducts recall effectiveness checks to verify that recalling firms notify theircustomers of the recall and that steps are taken to make certain that the product is no longer available to consumers.
Media outlets with questions regarding the recall can contact Arnold Avalos, VP of Operations, at 408-500-4118. Consumers with questions regarding the recall can contact Sandra Johnson, Sales Coordinator, at 408-500-4114.