Voluntary Recall Kogenate® FS 2000 IU Lots
Vials labeled as Kogenate® FS actually contain JIVI® antihemophilic factor (recombinant) PEGylated-aucl 3000 IU.
Please be advised that Bayer has issued a voluntary recall of Kogenate® FS 2000 IU vials.
According to the manufacturer, certain vials from the two lots listed below that were labeled as Kogenate® FS actually contain the FVIII hemophilia A treatment, JIVI® antihemophilic factor (recombinant) PEGylated-aucl 3000 IU. Bayer is requesting that the use of these lots be immediately discontinued.
|Lot Number||NDC||Expiry Date|
Returns are limited to the Kogenate® lots listed above.
Anyone with an existing inventory of Kogenate® should determine whether they have product from the recalled lots, quarantine and discontinue distribution of the affected product.
If you have affected lots of Kogenate®, please contact Wow! Customer Care to begin the returns process.
If you already received notification and returned the product to FFF Enterprises, no action is required.
For assistance, please call Wow! Customer Care at (800) 843-7477.