Class II
Medical Device Recall: Intellis AdaptiveStim Product Number 97715, Spinal Cord Stimulator
Medtronic Neuromodulation · March 28, 2024
Reason for Recall
inability to reprogram one device
Distribution
International distribution in the country of UK.
States Affected
IN
Quantity Affected
1 unit
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1691-2024
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.