FDA DevicesClass II
A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465 and 2....
Published: January 21, 2026Recall ID: Z-1043-2026Category: devicesCountry: US
Reason for Recall / Hazard
Complaints received that Vanta A71200 CP App does not function as intended during use. There is a potential for prolonged or postponed surgical procedure.
Product Description & Identification
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).
Affected Products
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).
Additional Source Details
| Field | Value |
|---|---|
| City | Minneapolis |
| State | MN |
| Event id | 98097 |
| Address 1 | 7000 Central Ave Ne |
| 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. |
| Postal code | 55432-3568 |
| Report date | 20260121 |
| Product type | Devices |
| Product quantity | 7123 |
| 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. |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20251203 |
| Initial firm notification | Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit |
| Center classification date | 20260109 |
Overview
- Recalling FirmMedtronic Neuromodulation
- StatusOngoing
- Risk LevelClass II
- DistributionWorldwide - US Nationwide distribution.