A71200 Vanta" Clinician Programmer Application (CP App)… recallZ-1043-2026 · Medtronic Neuromodulation · initiated Dec 3, 2025
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Medtronic Neuromodulation or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was 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.
FDA root cause category: Software design
What the company is doing
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.
Recall details
- Recall number
- Z-1043-2026
- Status
- Open, Classified
- Initiated by the company
- Dec 3, 2025
- Posted by the FDA
- Jan 9, 2026
- Recalling firm
- Medtronic Neuromodulation
- Quantity
- 7123
- Product code
- LGW
- FDA submissions
- P840001S594
- Distribution
- Worldwide - US Nationwide distribution.
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).
Code information (models, lots, serial numbers)
version 2.0.2465 and 2.0.2683 UDI-DI (GTIN) 00763000520083 Affected product is the software. Implanted Vanta Neurostimulator devices are not affected.
Devices named in this recall
1 device in the FDA device registry whose identifier appears in the recall's code information.
- N/A A71200Medtronic, Inc. · Stimulator, spinal-cord, totally implanted for pain relief1 recall0 reports
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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