Quick Facts at a Glance
- Recall Date
- December 3, 2025
- Hazard Level
- HIGH
- Brand
- Medtronic Neuromodulation
- Category
- Health & Personal Care
- Sold At
- Multiple Retailers
- Geographic Scope
- 1 states
- At-Risk Groups
- GENERAL
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- Medtronic Neuromodulation
- Product type
- Clinician Programmer Application
- Model 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.
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
December 3, 2025
Reported by FDA DEVICE
January 21, 2026
RecallRadar source check
January 28, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Complaints received that Vanta A71200 CP App does not function as intended during use. There is a potential for prolonged or postponed surgical procedure.
What You Should Do
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Medtronic Neuromodulation or your healthcare provider for instructions. Notification method: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
About This Product
The Vanta Clinician Programmer Application is used in medical settings to operate Vanta Neurostimulator devices during procedures. Healthcare providers rely on its functionality for safe and effective patient care.
Why This Is Dangerous
The software's inability to function correctly can lead to delays in surgical procedures, which can affect patient outcomes and overall surgical schedules.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
The recall necessitates immediate action from healthcare providers and patients, potentially impacting scheduled surgical procedures and patient care timelines.
Practical Guidance
How to identify if yours is affected
- Check the version number of your Vanta Clinician Programmer Application.
- If your version is 2.0.2465 or 2.0.2683, it is affected by the recall.
- Consult your healthcare provider for further assistance.
Where to find product info
Version numbers can typically be found within the application settings or on the device information screen.
What timeline to expect
Expect a response from the manufacturer or healthcare provider within 1-3 weeks regarding the recall procedure.
If the manufacturer is unresponsive
- Contact Medtronic Neuromodulation directly through their customer service line.
- Document all correspondence and keep records of your communications.
How to prevent similar issues
- Ensure that any medical software used is regularly updated to the latest version.
- Verify the software's compatibility with your medical devices before use.
- Consult with IT professionals in healthcare to assess software reliability.
Documentation advice
Keep records of any communications with the manufacturer, including emails and letters, as well as any receipts or documentation related to the software.
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Product Details
The recall affects Vanta Clinician Programmer Application versions 2.0.2465 and 2.0.2683. The product number is A71200, and it is deployed on Samsung tablets (CFN CT900). The software was distributed worldwide.
Key Facts
- Recalled software may delay surgical procedures
- Stop using the product immediately
- Contact healthcare provider for guidance
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Safety Guide
Not sure what to do next? Our guide walks you through the process step by step.
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