FDA tags Medtronic embolisation device recall as Class I
The US Food and Drug Administration (FDA) has tagged Medtronic’s recall of certain Pipeline Vantage embolisation devices as Class I following reports of four patient deaths. The post FDA tags Medtronic embolisation device recall as Class I appeared first on Medical Device Network.

The post FDA tags Medtronic embolisation device recall as Class I appeared first on Medical Device Network.