Penumbra 3D Stroke Revascularization Device Recalled Penumbra 3D Stroke Revascularization Device Recalled

The class I recall, posted today by the FDA, was issued because of the risk that wire material may break or separate during use.Medscape Medical News

Source: Medscape Medical News Headlines - July 21, 2017 Category: Consumer Health News Tags: Cardiology News Alert Source Type: news