Medtronic Model 37751 Recharger, in Charging Systems used with implantable neurostimulators (INS) Charging System Models 37754 & 97754, used with spinal cord stimulation (SCS) devices:- Restore- RestoreUltra- RestoreAdvanced- RestoreSensor- RestoreUltra SureScan MRI- RestoreAdvanved SureScan MRI- RestoreSensor SureScan MRIRecharger in Charging System kit Model 37651, used with deep brain stimulation (DBS) device: - Medtronic Activa RC
Modèle / numéro de série
Medtronic Model 37751 Recharger, in Charging Systems used with implantable neurostimulators (INS)Charging System Models 37754 & 97754, used with spinal cord stimulation (SCS) devices:- Restore- RestoreUltra- RestoreAdvanced- RestoreSensor- RestoreUltra SureScan MRI- RestoreAdvanved SureScan MRI- RestoreSensor SureScan MRIRecharger in Charging System kit Model 37651, used with deep brain stimulation (DBS) device: - Medtronic Activa RCARTG Number: 121279
“If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.