Medtronic Neuromodulation: Medical Device Recall in 2026 - (Recall #: Z-1043-2026)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2026.

Data Source: FDA.

Product Description:

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).

Product Classification:

Class II

Date Initiated: December 3, 2025

Date Posted: January 21, 2026

Recall Number: Z-1043-2026

Event ID: 98097

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.

Status: Ongoing

Product Quantity: 7123

Code Information:

version 2.0.2465 and 2.0.2683 UDI-DI (GTIN) 00763000520083 Affected product is the software. Implanted Vanta Neurostimulator devices are not affected.

Distribution Pattern:

Worldwide - US Nationwide distribution.

Voluntary or Mandated:

Voluntary: Firm initiated