DrugApr 3, 2013
CareFusion 213 SEPP 10% Povidone Iodine Solution USP recall — FDA D-226-2013
Labeling: Not Elsewhere Classified: This product is misbranded because the product is not sterile and the labeling is misleading in relation to sterility claims.
Class IIFDA: TerminatedCareFusion 213, LLC