Medtronic recalls Vanta Clinician Programmer App version 2.0.2455 for potential connection issues with patients using multiple neurostimulators. This software update may prevent proper communication with implantable devices.
Potential communication issue in which the Vanta Clinician Programmer Application (CP App) A71200 v2.0.2455 may be unable to connect with a Vanta Implantable Neurostimulator (INS) Model 977006 when a patient is implanted with more than one neurostimulator.
Medtronic is recalling a specific software version for programming their Vanta implantable neurostimulators. The issue could prevent the device from connecting properly if a patient has more than one neurostimulator implanted.
The software version 2.0.2455 may not communicate correctly with the Vanta implantable neurostimulator when multiple devices are present. This could lead to programming failures or improper device function.
Patients with Medtronic Vanta implantable neurostimulators who have more than one device implanted are likely affected. Those using the specific software version for programming are at risk of connection issues.
Check if you have the Vanta Clinician Programmer Application software version 2.0.2455. The product is for programming Medtronic Model 977006 Vanta implantable neurostimulators.
Download the latest software version from Medtronic's official website to resolve potential connection issues.
No, the recall does not require immediate discontinuation. Updating to the latest version resolves the issue.
The software may not connect properly with multiple devices, which could cause programming failures.
Yes, the software version 2.0.2455 is for Medtronic Model 977006 Vanta implantable neurostimulators.
We’ve drafted a message you can send Medtronic Neuromodulation to request your refund or repair — edit it as you like.
Subject: Recall Z-1574-2022 — Medtronic Neuromodulation Medtronic Neuromodulation Hello, I own a Medtronic Neuromodulation that is covered by recall Z-1574-2022 from Medtronic Neuromodulation. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
