|Announced||Manufacturer||Medication/Product Recall||Patient Guidance|
|January 20, 2021||CSL Behring||Monoline||Voluntary Product Recall Notification|
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Announced Manufacturer Medication/Product Recall Patient Guidance July 19, 2019 – Voluntary Recall BAYER Kogenate FS – View FDA Website Patients are instructed to direct questions regarding the recall, risks, or possible adverse effects from this medication, to their physician or their local Hemophilia Treatment Center. Patients may also contact the FDA at 1-800-332-1088 or visit the FDA's website for further information.