PlainRecalls
FDA Devices Moderate Class II Ongoing

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).

Reported: January 21, 2026 Initiated: December 3, 2025 #Z-1043-2026

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).

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.

Details

Recalling Firm
Medtronic Neuromodulation
Units Affected
7123
Distribution
Worldwide - US Nationwide distribution.
Location
Minneapolis, MN

Frequently Asked Questions

What product 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).. Recalled by Medtronic Neuromodulation. Units affected: 7123.
Why was this product 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.
Which agency issued this recall?
This recall was issued by the FDA Devices on January 21, 2026. Severity: Moderate. Recall number: Z-1043-2026.