GE Healthcare recalls Centricity Universal Viewer 6.0 software versions that may display incorrect patient images from Enterprise Archive or VNA due to missing updated studies. Affected units include specific software versions and model numbers.
There is the possibility of viewing studies directly from the Enterprise Archive or VNA with incorrect patient images because the updated series or study is not present in the archive.
GE Healthcare is recalling Centricity Universal Viewer 6.0 software versions that could show incorrect patient images when viewing studies from the Enterprise Archive or VNA. This risk occurs because updated studies might not be present in the archive, potentially leading to misdiagnosis.
The device may display incorrect patient images when viewing studies from the Enterprise Archive or VNA because updated study series or individual studies are not properly stored in the archive. This could lead to misdiagnosis if healthcare providers rely on the incorrect images for patient care.
Healthcare providers using the Centricity Universal Viewer 6.0 software versions listed in the recall. Medical professionals who rely on this device for displaying patient images are most at risk.
Check for the model number 2098249-002 and software versions listed in the recall, including 6.0.9, 6.0SP9.01, and other specific versions. The device is sold by GE Healthcare and used in healthcare settings.
Review the software version on your Centricity Universal Viewer to see if it matches the listed versions in the recall.
The affected software versions include 6.0.9, 6.0SP9.01, CPACS 6.0 SP9.0.1, UV 6.0 SP9.0.1, UV 6.0 SP9.01.1, UV 6.0 SP9.0.1.2, UV 6.0 SP9.01.3, UV6.0 SP9.01.4, UV 6.0 SP9.01.5, UV 6.0 SP9.0.1.6, UV Version 6.0 SP5.0.4.1, UV Version 6.0 SP9, UV Version 6.0 SP9.0.0.1, UV Version 6.0 SP901, UV Version 6.0 SP9011, and UV Version 6.0 SP902.
Check for the model number 2098249-002 and the specific software versions listed in the recall. The device is used in healthcare settings and displays medical images.
The recall does not specify a remedy, so you should check the software version and 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-1910-2019 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-1910-2019 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.
