Bayer Recalls Two Lots of Kogenate 2000 Iu Vials in U.S.: FDA

Bayer is voluntarily recalling two lots of Kogenate FS antihemophilic factor 2000 IU vials in U.S. to the patient level, FDA said in a statement.

• Certain vials from these two lots that were labeled as Kogenate FS actually contain the FVIII hemophilia A treatment, Jivi antihemophilic factor PEGylated-aucl 3000 IU, it said

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