GE Healthcare recalls Centricity Universal Viewer Zero Footprint Client versions with incomplete patient imaging study display. Affected units may need software update to prevent image display issues.
There is a potential to display incomplete patient imaging study.
GE Healthcare is recalling certain versions of their Centricity Universal Viewer software. This version may display incomplete patient imaging studies, which could lead to incorrect medical decisions if not addressed.
The software may display incomplete patient imaging studies. This could lead to incorrect medical decisions if healthcare providers rely on the incomplete images for diagnosis or treatment planning.
Healthcare facilities using the recalled software versions are most at risk. Patients receiving imaging studies through these systems could potentially see incomplete images.
Check if your Centricity Universal Viewer Zero Footprint Client is version 6.0 SP9 through SP10.2.2.1. The product has GTIN 00840682102988 and UDI 00840682102988.
Identify your software version by checking the Centricity Universal Viewer Zero Footprint Client settings.
The recall indicates a potential to display incomplete patient imaging studies, but it does not specify a risk of serious injury or death. This is considered a low-risk issue.
Check if your Centricity Universal Viewer Zero Footprint Client is version 6.0 SP9 through SP10.2.2.1, as listed in the recall notice.
The recall does not specify a remedy, so you should check your software version and contact GE Healthcare for 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-0329-2022 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-0329-2022 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.
