Recall Z-1691-2024— Medtronic Neuromodulation
Class II · Ongoing
Class II FDA medical device recall by Medtronic Neuromodulation, initiated 2024-03-28. FDA's recall record names no specific 510(k) clearance for this event. Product: Intellis AdaptiveStim Product Number 97715, Spinal Cord Stimulator. Reason: inability to reprogram one device.
- Recalling firm
- Medtronic Neuromodulation
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2024-03-28
- Firm location
- Minneapolis, MN, United States
Product description
Intellis AdaptiveStim Product Number 97715, Spinal Cord Stimulator
Reason for recall
inability to reprogram one device
Data sourced from openFDA. This site is unofficial and independent of the FDA.