FDA: Class I Recall of 48 Medtronic ICDs, CRT-Ds FDA: Class I Recall of 48 Medtronic ICDs, CRT-Ds

Clinicians received serial numbers in January and were asked to consider replacement of the affected devices, said to have a manufacturing defect that might prevent shock or pacing therapy.News Alerts

Source: Medscape Medical News Headlines - February 27, 2018 Category: Consumer Health News Tags: Cardiology News Alert Source Type: news