date:Apr 05, 2012
hange was not reflected on the finished product label. The problem was discovered during a routine verification activity by FSIS. FSIS and the company have not received any 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 that recalling firms notify their customers of the recall and steps are taken to ensure the product is no longer available to