A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465 and 2.0.2683, Product number A71200. Software i
FDA device recall Z-1043-2026 · posted 2026-01-09 · Open, Classified
Recall details
- Recalling firm
- Medtronic Neuromodulation
- 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.
- 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.
- Root cause
- Software design
- Status
- Open, Classified
- Product code
- LGW
- Quantity affected
- 7123
- Distribution
- Worldwide - US Nationwide distribution.
- Date initiated
- 2025-12-03
- Date posted
- 2026-01-09
- Location
- Minneapolis, MN
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