FDAJuly 31, 2026
GE Healthcare Workflow Core Services V8 Recall Over Patient Data Association Issue
FDA published this notice on July 31, 2026 for United States.
This notice is kept at its address for anyone who saved the link. AreaZine no longer holds the agency's full record for it, so the page shows what AreaZine recorded and links to the agency's own page, the one to read.
What AreaZine recorded
- Agency
- FDA
- Place
- United States
- Date
- July 31, 2026
- Recall class
- Class II
- Reason given by the agency
- Under certain conditions historical imaging data migrated from a legacy system may become incorrectly associated with a different patient. If this occurs, studies or images may be displayed under the wrong patient record, which could lead to misdiagnosis or a delay in patient care.
- Distribution
- Worldwide - US Nationwide distribution.
- Official source
- the notice at its source
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Source: FDA.