Medtronic Neurological
Minneapolis, MN
This page shows every FDA and USDA recall linked to Medtronic Neurological. Each entry includes the product involved, when the recall happened, and how serious it was. If a company has had multiple recalls over the years, you can see the full history here in one place — including whether any were Class I, which is the most serious type.
6
Total Recalls
2006
First Recall
2006
Most Recent
Medtronic Kinetra Dual Program Neurostimulator for Deep Brain Stimulation, model 7428. Rx only. Medtronic, I...
Dec 19, 2006
· Device
Terminated
Medtronic 3777 Lead Kit, 1x8 Low Impedance Lead Kit for Spinal Cord Stimulation (SCS). Manufactured at: Med...
Sep 29, 2006
· Device
Terminated
Medtronic 3778 Lead Kit, 1x8 Compact Low Impedance Lead Kit for Spinal Cord Stimulation (SCS). Manufactured...
Sep 29, 2006
· Device
Terminated
Medtronic Intrathecal Catheter Distal Revision Kit, Model 8598, (provides replacement parts for the distal sec...
Sep 9, 2006
· Device
Terminated
Medtronic Intrathecal Catheter, Model 8731, (part of infusion systems using Medtronic implantable pumps) The...
Sep 9, 2006
· Device
Terminated
Medtronic Kinetra 7428. Dual Program Neurostimulator for Deep Brain Stimulation. Rx only. Medtronic, Inc.,...
May 27, 2006
· Device
Terminated