130,000 pounds of - vacuum pack plastic bags of Bo Vien recalled over undeclared allergen

Recall date

January 17, 2014

Source

U.S. Department of Agriculture (USDA FSIS)

Official notice title

Colorado Firm Recalls Beef and Pork Products Due To Misbranding and Undeclared Allergen

Recall number

004-2014

FDA classification

Class II

Brand / firm

Huong Duyen Meat Products

Sold / distributed

California, Colorado, Illinois

Why it was recalled

Misbranding; Unreported Allergens

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

WASHINGTON, Jan. 17, 2014 European Meat Products Inc., a Lakewood, Colo., establishment, is recalling approximately 130,000 pounds of fresh and ready-to-eat beef and pork products because of misbranding and an undeclared allergen, the U.S. Department of Agriculture's Food Safety and Inspection Service (FSIS) announced today. The products contain wheat, a known allergen which is not declared on the labels. The products subject to recall include: 16 oz. - vacuum pack plastic bags of iBo Vien, Huong Duyen Cooked Beef Meat Balls” 100 oz. - vacuum pack plastic bags of iBo Vien, Huong Duyen Cooked Beef Meat Balls” 16 oz. vacuum pack plastic bags of iCha Chien, Huong Duyen Pork Meat Roll Browned in Soy Bean Oil” 16 oz. - plastic tubs of iMoc TUOi, Huong Duyen Fresh Pork Paste” 16 oz. - vacuum pack plastic bags of iGio-Lua, Huong Duyen Pork Meat Roll” 32 oz. - vacuum pack plastic bags of iGio-Lua, Huong Duyen Pork Meat Roll” The products bear the establishment number iEST. 7725” inside the USDA Mark of Inspection. The recalled products were produced prior to January 17, 2014. The products were shipped to distributors, restaurants and retail establishments in California, Colorado, and Illinois. The problem was discovered by FSIS during a routine food safety assessment label review. The problem occurred due to a change in ingredient formulation without a corresponding change in the finished product label. 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 healthcare provider. FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. Consumers and media with questions about the recall should contact Phong Tong, a company executive, at (303) 233-3111. Consumers with food safety questions can iAsk Karen,” the FSIS virtual rep…