GE Healthcare recalls Centricity Universal Viewer with PACS-IW foundation 6.0.x displays due to synchronization failure. Affected units include specific model numbers and installation IDs. Consumers should check their device details to determine if recalled.
Synchronization failure
GE Healthcare is recalling certain Centricity Universal Viewer displays that use PACS-IW foundation 6.0.x software. The recall is due to a synchronization failure that could cause medical images and data to not display correctly. This may affect the accuracy of mammograms and other medical imaging results.
Synchronization failure means the device may not properly display medical images or data from imaging sources. This could lead to incorrect or missing information for mammograms and other medical imaging results, potentially affecting diagnosis and treatment decisions.
Healthcare facilities using the Centricity Universal Viewer with PACS-IW foundation 6.0.x software are most at risk. Patients receiving mammograms or other medical imaging through these devices could be affected if the display fails.
Check for specific model numbers and installation IDs listed in the recall notice. Affected units include the Centricity Universal Viewer with PACS-IW foundation 6.0.x software and specific serial numbers like 303715CVUWTSW or 918277CVUWBSW.
Review the model number and installation ID on your device to see if it matches the listed serial numbers in the recall notice.
The displays have a synchronization failure that may cause medical images and data from imaging sources to not display correctly.
Check for specific model numbers and installation IDs listed in the recall notice, such as 303715CVUWTSW or 918277CVUWBSW.
If your device does not match the listed model numbers or installation IDs, it is not affected by this recall.
We’ve drafted a message you can send GE Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-0375-2019 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-0375-2019 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.
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.
