Medtronic Neuromodulation recalled 7,123 units of the Vanta Clinician Programmer Application on December 3, 2025. The software may not function as intended, potentially delaying surgical procedures. Healthcare providers and patients must stop using the software immediately.
Complaints received that Vanta A71200 CP App does not function as intended during use. There is a potential for prolonged or postponed surgical procedure.
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
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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.
The software's inability to function correctly can lead to delays in surgical procedures, which can affect patient outcomes and overall surgical schedules.
This recall is not part of a broader industry pattern.
The recall necessitates immediate action from healthcare providers and patients, potentially impacting scheduled surgical procedures and patient care timelines.
Version numbers can typically be found within the application settings or on the device information screen.
Expect a response from the manufacturer or healthcare provider within 1-3 weeks regarding the recall procedure.
Keep records of any communications with the manufacturer, including emails and letters, as well as any receipts or documentation related to the software.
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.
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