April 25, 2011 – The Food and Drug Administration has announced additional warnings to be included on the labels and literature regarding the popular drug Tysabri. On April 22nd, the FDA posted new updates to the...
Defective Penumbra Reperfusion Catheters Recalled
December 14, 2010 – Penumbra, in cooperation with the U.S. Food and Drug Administration (FDA), has initiated a voluntary safety recall of the Penumbra System Reperfusion Catheter 032. The function of the Penumbra System...