RecallDepth

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).

Company
Medtronic Neuromodulation
Recall Initiated
December 3, 2025
Posted
January 9, 2026
Recall Number
Z-1043-2026
Quantity
7123
Firm Location
Minneapolis, MN

Reason for Recall

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

Distribution

Worldwide - US Nationwide distribution.

Lot / 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.

Root Cause

Software design

Action Taken

On December 3, 2025 the firm distributed Urgent Medical Device Safety Notification letters to affected consignees. Customers were instructed to download and install A81200 CP App v2.0.2684 or any later version.

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