GE Medical Systems recalls Centricity Universal Viewer 6.0 software that may hide medical studies without user notification, potentially delaying diagnosis. Affected units have specific product IDs listed in the recall.
There is the potential that after installation of the IAS tool, some studies can remain hidden without user notification. Access to those hidden studies requires GE Healthcare assistance, which can result in a delay in reading the study.
GE Medical Systems is recalling Centricity Universal Viewer 6.0 software that may hide medical studies (including mammograms) without user notification. This could delay diagnosis if the hidden studies require GE Healthcare assistance to access.
After installing the IAS tool, some medical studies can remain hidden without user notification. Access to these hidden studies requires GE Healthcare assistance, which may delay reading the study and potentially impact timely diagnosis.
Healthcare providers using Centricity Universal Viewer 6.0 software for medical imaging, particularly those handling mammograms. Patients whose studies are hidden may face delayed diagnosis.
Check for product IDs listed in the recall: 100666-1-Centricity Universal Viewer-14194768, 100666-1-Centricity Universal Viewer-20084199, and other specific serial numbers provided in the recall notice.
Look for the specific product IDs listed in the recall notice to confirm if your software is affected.
The recall states that after installing the IAS tool, some medical studies can remain hidden without user notification, which may delay diagnosis if the hidden studies require GE Healthcare assistance to access.
Check for the specific product IDs listed in the recall notice, such as 100666-1-Centricity Universal Viewer-14194768 or other serial numbers provided in the recall.
The recall does not specify a remedy, so affected users should check with GE Healthcare for assistance accessing hidden studies.
We’ve drafted a message you can send GE Medical Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-0722-2023 — GE Medical Systems GE Medical Systems Hello, I own a GE Medical Systems that is covered by recall Z-0722-2023 from GE Medical Systems. 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.
