Endologix Broadens Recall to All AFX Endovascular AAA Systems Endologix Broadens Recall to All AFX Endovascular AAA Systems

The company is recalling all AFX endovascular aortic aneurysm systems after continued problems with type III endoleaks. The FDA has now classified the recall as class I, the most serious designation.News Alerts
Source: Medscape Medical News Headlines - Category: Consumer Health News Tags: Cardiology News Alert Source Type: news