Bayer Recall of Two Lots of Kogenate FS
Bayer has announced a recall of two lots of Kogenate® FS 2000 IU vials. Within these two lots there were certain vials labeled as Kogenate FS but actually contain FVIII hemophilia A treatment, Jivi® antihemophilic factor (recombinant_ PEGylated-aucl 3000 IU). This recall is only in the United States where affected products were distributed. For more information about the recall including the affected lots and instructions for patients who received vials from either of the affected lots, please visit the links below.