Edwards Lifesciences Recalls Devices After 3 Deaths Reported

Edwards Lifesciences Recalls Devices After 3 Deaths Reported

Source: 
RAPS.org
snippet: 

The US Food and Drug Administration (FDA) recently announced a Class I recall of more than 700 Edwards Lifesciences’ IntraClude Intra-Aortic Occlusion Devices after receiving 22 complaints related to balloon rupture or puncture, including three deaths.