Medtronic recalls Vanta Clinician Programmer App version 2.0.2455 for pain therapy devices that may show error 1502, preventing programming of implantable neurostimulators.
Potential for Vanta Clinician Programmer Application (CP App) A71200 v2.0.2455 to display an Unexpected Device Error Code 1502 Message, and the user will be unable to perform programming of the Vanta Implantable Neurostimulator (INS) Model 977006.
Medtronic is recalling its Vanta Clinician Programmer Application software version 2.0.2455 for pain therapy devices. This version may display an error message that prevents users from programming their implantable neurostimulators, which could lead to improper device settings.
The software version 2.0.2455 may display an error message (code 1502) that prevents users from programming the implantable neurostimulator. This could lead to improper device settings if users try to update or adjust the device without the software working correctly.
Users of Medtronic Vanta implantable neurostimulators for pain therapy who have the Vanta Clinician Programmer Application software version 2.0.2455 are likely affected. Patients with these devices who need to adjust their neurostimulator settings are at most risk.
Check if you have the Vanta Clinician Programmer Application software version 2.0.2455 for Medtronic Model 977006 Vanta implantable neurostimulators used in pain therapy.
Download the updated software version from Medtronic's website to fix the error message issue.
No, the software issue only prevents programming of the device and does not cause harm directly.
Check if you have the Vanta Clinician Programmer Application software version 2.0.2455 for Medtronic Model 977006 Vanta implantable neurostimulators used in pain therapy.
Download the updated software version from Medtronic's website to fix the error message issue.
We’ve drafted a message you can send Medtronic Neuromodulation to request your refund or repair — edit it as you like.
Subject: Recall Z-1571-2022 — Medtronic Neuromodulation Medtronic Neuromodulation Hello, I own a Medtronic Neuromodulation that is covered by recall Z-1571-2022 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.
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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.
