Class I Recall of Medtronic DBS Lead Kits Class I Recall of Medtronic DBS Lead Kits

The FDA has classified a notification by Medtronic to physicians about potential complications with the lead cap in its lead kits and dystonia therapy kits a class I recall. News Alerts
Source: Medscape Today Headlines - Category: Consumer Health News Tags: Neurology & Neurosurgery News Alert Source Type: news