Class II

Medical Device Recall: Vanta Implantable Neurostimulator (INS), Model 977006

Medtronic Neuromodulation · August 21, 2024

Reason for Recall

Model 977006 Vanta INS batterty life has depleted faster than HCPs or patients expected leading to outpatient reprogramming or earlier than anticipated surgical replacements.

Distribution

Worldwide distribution.

Quantity Affected

11789 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0132-2025

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.