Medtronic Neuromodulation recalls A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465 and 2.0.2683, Product number A71200. Software…

Recall date

December 3, 2025

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-1043-2026

FDA classification

Class II

Brand / firm

Medtronic Neuromodulation

Sold / distributed

Worldwide - US Nationwide distribution.

Why it was recalled

Complaints received that Vanta A71200 CP App does not function as intended during use. There is a potential for prolonged or postponed surgical procedure.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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).