date:May 26, 2012
ide the USDA mark of inspection.
These products were sold to consumers at the company's retail store.
FSIS noted that the problem was identified by FSIS during a routine label review. The problem may have occurred due to a change in suppliers.
FSIS and the company have not received reports of adverse reactions due to consumption of these products. The agency has advised anyone concerned about a reaction to contact a healthcare provider.