Medtronic NIM Vital Nerve Monitoring System Recall Issued After Injuries Reported
FDA determined a Medtronic device correction notice constituted a NIM Vital Nerve Monitoring System recall, following at least 10 reports of patient injuries.
FDA determined a Medtronic device correction notice constituted a NIM Vital Nerve Monitoring System recall, following at least 10 reports of patient injuries.
The new handpiece allows the Renuvion/J-Plasma device to be used for a limited number of cosmetic surgery procedures.
Cosmetic skin surgery complications from Renuvion/J-Plasma devices may include burns, nerve damage, and other injuries the FDA warns.