date:Oct 12, 2017
egulations by, among other deficiencies, failing to adequately control the risk of Listeria monocytogenes and Clostridium botulinum toxin formation in their vacuum-packed fish or fishery products.
FDAs testing of environmental samples revealed Listeria monocytogenes in multiple locations throughout the facility. Those samples were collected in January 2016 and in July 2016. The FDA alleges that the defendants did not manufactured, package, and store goods under conditions necessary to minimize