WhichRecall
Class IIReported 2026-01-21

A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465 and 2.0.2683, Product number A71200. Software is deployed and operated on Samsung tablets (CFN CT900).

Recalled by Medtronic Neuromodulation

Reason for Recall

Complaints received that Vanta A71200 CP App does not function as intended during use

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There is a potential for prolonged or postponed surgical procedure.

Recall Number
Z-1043-2026
Classification
Class II
Status
Ongoing
Category
device
Initiated
2025-12-03
Reported
2026-01-21
Distribution
Worldwide - US Nationwide distribution.
Code Info
version 2.0.2465 and 2.0.2683 UDI-DI (GTIN) 00763000520083 Affected product is the software. Implanted Vanta Neurostimulator devices are not affected.
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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