FDAAugust 21, 2024device

Vanta Implantable Neurostimulator (INS), Model 977006

Official recall recorded by the U.S. Food & Drug Administration.

The 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.

What to do

FDA enforcement status: Ongoing

Brands named

medtronic neuromodulationmedtronic

UPCs

00763000411923

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Vanta Implantable Neurostimulator (INS), Model 977006 — Recall Details · AllClear