GE Healthcare recalls SIGNA Voyager MRI systems with software versions VX29.1 and PX26.4 (China only) due to potential missing slices causing gaps in 3D anatomy images. Affected units may require software updates to prevent imaging errors.
Under certain conditions, some slices may be missing which can lead to a gap of anatomy in the 3D Volume images.
GE Healthcare is recalling some SIGNA Voyager MRI systems because certain software versions can cause gaps in 3D images during scans. This could lead to inaccurate medical imaging results if not corrected.
The software issue causes some slices to be missing during MRI scans, creating gaps in the 3D images. This can result in incomplete anatomical views that might affect diagnosis accuracy.
Medical facilities using SIGNA Voyager MRI systems with software versions VX29.1 or PX26.4 (China only) are affected. Patients undergoing scans on these systems may face inaccurate imaging results.
Check if your SIGNA Voyager MRI system has software version VX29.1 or PX26.4 (China only). The software version is typically found in the system's settings or documentation.
Identify your MRI system's software version to see if it matches VX29.1 or PX26.4 (China only).
The recall is due to a software issue that can cause missing slices in 3D images, potentially leading to inaccurate anatomical views.
Check your SIGNA Voyager MRI system's software version; affected units have VX29.1 or PX26.4 (China only).
The official recall does not specify a remedy or action for affected systems. Contact GE Healthcare for further guidance.
We’ve drafted a message you can send GE Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0138-2022 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-0138-2022 from GE Healthcare. 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.
