Official recall record

Vanta Implantable Neurostimulator (INS)

Health Canada — Medical Devices · 2024-08-26 · CanadaType I

Issuing authority: Health Canada — Medical Devices
Published: 2024-08-26
Country of alert: Canada
Alert level: Type I
Alert type: recall

What the authority reported

The purpose of this recall is to emphasize the impact programming settings can have on the battery life of the Vanta Implantable Neurostimulator (INS) model 977006. Additionally, this letter is intended to remind you of the tools that currently exist in both models A71200 Vanta Clinician Programmer application and A71300 Stimulation Trialing Clinician Programmer application. These tools should be used to assist in selecting the appropriate INS model for the patient and to assess the longevity of the Vanta INS throughout the life of the implant. Recall start date: August 20, 2024

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

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