BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Safety Notice for application and recall of DBS Extensions Kits

Product group Active implantable medical devices - biostimulators
Reference 07585/12

Urgent Field Safety Notice for application and recall of DBS Extensions Kits, Models 37085, 37086 and 7482, of Medtronic Inc., Minneapolis, USA, due to possible risk of faulty connector boots.

Safety Notice for application and recall of DBS Extensions Kits , Download_VeroeffentlichtAm_EN PDF, 94KB, File does not meet accessibility standards