date:Feb 13, 2014
and a date on the packages prior to August 11, 2015, in the format of mm dd yy.
The problem was discovered by an FSIS in-plant inspector during a label review. The firm believed the releasing agent was a processing aid that did not need to be declared on the 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