Medtronic Neuromodulation - Medtronic, External neurostimulator - Class 2 Recall

Medtronic, External neurostimulator, ENS (37021) & ENS (37022). All Restore, PrimeAdvanced¿ and Itrel 4 devices are used for Spinal Cord Stimulation. All Activa devices are used for Deep Brain Stimulation. Restore¿ (Model 37711), the first released affected product was released to the market in April, 2005. There are a total of 19 affected device models, including the external neurostimulators which are associated with software application run on the NVision¿ Clinician Programmer and used during trialing for spinal cord stimulation (SCS) patients.
Source: Medical Device Recalls - Category: Medical Equipment Source Type: alerts