PlainRecalls
FDA Devices Moderate Class II Terminated

Medtronic Activa RC (37612), Activa PC (37601), Activa SC (37602), Activa SC (37603), Activa PC+S (37604), Multi-program Rechargeable Neurostimulator for Deep Brain Stimulation for movement disorders.

Reported: May 7, 2014 Initiated: February 27, 2014 #Z-1525-2014

Product Description

Medtronic Activa RC (37612), Activa PC (37601), Activa SC (37602), Activa SC (37603), Activa PC+S (37604), Multi-program Rechargeable Neurostimulator for Deep Brain Stimulation for movement disorders.

Reason for Recall

Medtronic neurostimulators (used with pain and deep brain stimulation therapy) have a cycling feature that, when enabled, allows stimulation output to be toggled on and off based on the programmed settings. The use of this feature is determined by the physician and set using the clinician programmer. Current labeling indicates the use of cycling improves device longevity and recharge interval

Details

Recalling Firm
Medtronic Neuromodulation
Units Affected
170,286 US, 73,921 OUS for all devices
Distribution
Nationwide Distribution - all states including DC and Puerto Rico.
Location
Minneapolis, MN

Frequently Asked Questions

What product was recalled?
Medtronic Activa RC (37612), Activa PC (37601), Activa SC (37602), Activa SC (37603), Activa PC+S (37604), Multi-program Rechargeable Neurostimulator for Deep Brain Stimulation for movement disorders.. Recalled by Medtronic Neuromodulation. Units affected: 170,286 US, 73,921 OUS for all devices.
Why was this product recalled?
Medtronic neurostimulators (used with pain and deep brain stimulation therapy) have a cycling feature that, when enabled, allows stimulation output to be toggled on and off based on the programmed settings. The use of this feature is determined by the physician and set using the clinician programmer. Current labeling indicates the use of cycling improves device longevity and recharge interval
Which agency issued this recall?
This recall was issued by the FDA Devices on May 7, 2014. Severity: Moderate. Recall number: Z-1525-2014.