Santa Maria Foods, a Brampton, Ontario, establishment, is recalling approximately 2,600 pounds of whole boneless ham prosciutto product due to possible contamination with Listeria monocytogenes, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced.

The ham product was shipped to California and Michigan for further distribution. Case labels bear the Canadian establishment number “473A” within the Canadian mark of inspection. The following product is subject to recall: Approximately 50-lb. boxes labeled “PROSCIUTTO x 4 GOLD” with the case codes BR031356 or BR031374, produced on Nov. 14 and Nov. 15, 2013. Each box contains 4 individually packaged hams with the case codes BR031341 or BR031354.

The problem was discovered by FSIS sampling collected during routine reinspection. The sampled product was held, but further investigation by Santa Maria Foods revealed that additional potentially implicated product had been released into commerce. FSIS and the company have received no reports of illnesses associated with consumption of these products.

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StockPot Inc., an Everett, Wash. establishment, is recalling 1,864 cases (approximately 22,368 pounds) of chicken noodle soup due to misbranding and an undeclared allergen. The Classic Chicken Noodle Soup product is formulated with wheat, a known allergen.  However, the product was released with a Loaded Baked Potato Style Soup side label, which does not declare this allergen.

The product subject to recall includes 24-oz. plastic tubs of Wholesome@Home “Classic Chicken Noodle Soup.” The establishment number “P-18235” is located on the label on the lid. The products were produced on October 25 and 26, 2013, with a use-by date of February 17 and 18, 2014. The product was shipped to distribution centers in the following states: Arizona, California, Colorado, Indiana, Oregon, Texas, Utah and Washington. The product was sold at retail only.

The problem was reported by a supermarket employee who noticed the labeling error while stocking shelves. The problem occurred when a subset of the labels provided by the label printing company were assembled incorrectly.  FSIS and the company have received no reports of adverse reactions due to consumption of these products.

Source: FSIS