Medtronic recalls version 1.0.4232 of the Restore Clinician Programmer Application Software (model A71100) due to compatibility issues with some legacy software, preventing communication with implanted neurostimulators.
The original version of the A71100 Restore Clinician Programmer Application has been identified to have a compatibility issue with some legacy clinician programmer software resulting in the programmer having an inability to establish communication with the implanted neurostimulators.
Medtronic is recalling version 1.0.4232 of the Restore Clinician Programmer Application Software (model A71100) because it has compatibility issues with some legacy software. This prevents the programmer from communicating with implanted neurostimulators, which could lead to improper device function.
The software version 1.0.4232 has a compatibility issue with some legacy clinician programmer software. This prevents the programmer from establishing communication with the implanted neurostimulators, which could result in improper device function.
Users of the Restore Neurostimulators who have the A71100 software version 1.0.4232 are affected. Patients with implanted neurostimulators are at risk if the software fails to communicate properly.
Check if you have the Restore Clinician Programmer Application Software version 1.0.4232 (model A71100) used with Restore Neurostimulators. The software was sold with the device and has a UDI-DI number 00763000273668.
Verify the software version by checking the device's settings or documentation for version 1.0.4232 (model A71100).
The specific software version being recalled is 1.0.4232 (model A71100).
The software issue prevents the programmer from communicating with implanted neurostimulators, which could lead to improper device function.
The recall record does not mention a remedy or fix.
We’ve drafted a message you can send Medtr: a short, human brand name for headings (e.g. "Trsmima") to request your refund or repair — edit it as you like.
Subject: Recall Z-2657-2023 — Medtr: a short, human brand name for headings (e.g. "Trsmima") Medtr: a short, human brand name for Hello, I own a Medtr: a short, human brand name for headings (e.g. "Trsmima") that is covered by recall Z-2657-2023 from Medtr: a short, human brand name for headings (e.g. "Trsmima"). 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.
