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Medtronic Neuromodulation recalls Vanta Implantable Neurostimulator (INS), Model 977006
Recalled October 23, 2024 · FDA recall Z-0132-2025 · Medtronic Neuromodulation
Hazard
Model 977006 Vanta INS batterty life has depleted faster than HCPs or patients expected leading to outpatient reprogramming or earlier than anticipated surgical replacements. · FDA Class II
Units
11789 units
Sold at
Worldwide distribution.
Description
Model 977006 Vanta INS batterty life has depleted faster than HCPs or patients expected leading to outpatient reprogramming or earlier than anticipated surgical replacements.
Product
Vanta Implantable Neurostimulator (INS), Model 977006
Manufacturer(s)
Medtronic Neuromodulation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →