GE Healthcare recalls SIGNA Artist MRI systems with software version DV29.1 due to potential missing slices causing gaps in 3D anatomy images. Affected units may require software update 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 SIGNA Artist MRI systems with software version DV29.1 because some slices may be missing, creating gaps in 3D images. This could lead to inaccurate medical imaging results if the system is used without correction.
The software version DV29.1 may cause some slices to be missing during imaging, creating gaps in the 3D volume images. This could result in incomplete or inaccurate anatomical representations in medical scans. The risk is specific to the software version and not present in all MRI systems.
Medical facilities using SIGNA Artist MRI systems with software version DV29.1 are most likely affected. Patients undergoing scans with these systems may experience inaccurate results if the issue isn't corrected.
Check if your SIGNA Artist MRI system has software version DV29.1. The recall applies to systems sold with this specific software version.
Verify your SIGNA Artist MRI system's software version to see if it is DV29.1.
The recall is for potential missing slices causing gaps in 3D images, but it does not pose a risk of serious injury or death. The hazard is specific to imaging accuracy.
The official recall does not specify a fix. Affected units may need to update the software to a newer version to resolve the issue.
Check your software version. If it is DV29.1, contact GE Healthcare for guidance on next steps.
We’ve drafted a message you can send GE Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0139-2022 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-0139-2022 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.
