GE Healthcare recalls Centricity PACS software version 7.0 SP0.0.4.7 due to failure to process study modification notifications on post-verified exams. Affected units include model 5831882-012 with GTIN 00840682145572.
The Event Notification Manager (ENM) functionality for certain products does not process notifications for study modifications performed on post verified exams.
GE Healthcare is recalling Centricity PACS software version 7.0 SP0.0.4.7 because it fails to process notifications for study modifications on post-verified exams. This could lead to missing critical updates in medical imaging systems, potentially affecting patient care.
The software fails to process notifications when study modifications are made after exams have been verified. This means critical updates to imaging studies might not be reflected in the system, potentially causing errors in patient records or treatment plans.
Healthcare facilities using the recalled software version are affected. Medical staff handling imaging studies may be at risk if notifications for study modifications are not processed correctly.
Check if your Centricity PACS software is version 7.0 SP0.0.4.7 with model number 5831882-012 or GTIN 00840682145572. The software was sold with these specific identifiers.
Verify your Centricity PACS software version by checking the model number or GTIN on the device.
The recall indicates a potential issue with study modification notifications, but the official notice does not specify if this causes immediate patient harm.
Check for model number 5831882-012 or GTIN 00840682145572 with software version 7.0 SP0.0.4.7.
The official recall does not specify a remedy, so check with GE Healthcare for further instructions.
We’ve drafted a message you can send GE Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1466-2022 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-1466-2022 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.
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.
