Enterprise Imaging XERO Viewer (Agfa) – Image Placement Bug (2024)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Enterprise Imaging XERO Viewer- software application used for reference and diagnostic viewing of multispecialty medical imaging and non-imaging data . Enterprise Imaging XERO Viewer 8.0.0, 8.0.1, 8.1, 8.1.1, 8.1.2, 8.1.3,8.1.4, 8.2.0.000, 8.2.1.000, 8.2.2.000, 8.3.0.000, 8.3.1.000, 8.3.2.000, 8.4.0.000, 8.4.1.000 (including all SU s and HF s)
Brand
Agfa Healthcare NV Septestraat 27 Mortsel Belgium
Lot Codes / Batch Numbers
8.4.1, 8.3.2, 8.3.1, 8.3.0, 8.2.2, 8.2.1, 8.2.0, 8.1.5, 8.1.4, 8.1.3, 8.1.2, 8.1.1, 8.1, 8.0.1, 8.0.0, ICIS View 2014.1, ICIS View 2014.2
Products Sold
UDI-DI: 05400874000710 Software Versions affected: All versions of Enterprise Imaging XERO Viewer are affected 8.1.2 or higher 8.1.4 or higher 8.2.0.100 or higher 8.2.2.000 or higher 8.3.2.000 or higher 8.4.0.000 or higher Enterprise Imaging XERO Viewer main version streams 8.4.0, 8.4.1, 8.3.2, 8.3.1, 8.3.0, 8.2.2, 8.2.1, 8.2.0, 8.1.5, 8.1.4, 8.1.3, 8.1.2, 8.1.1, 8.1, 8.0.1, 8.0.0, ICIS View 2014.1, ICIS View 2014.2
Agfa Healthcare NV Septestraat 27 Mortsel Belgium is recalling Enterprise Imaging XERO Viewer- software application used for reference and diagnostic viewing of mu due to Software defect, when an image has non-square pixel spacing, the reference/localizer line is incorrectly placed on the scout image in the XERO Viewet,. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Software defect, when an image has non-square pixel spacing, the reference/localizer line is incorrectly placed on the scout image in the XERO Viewet, may display the incorrect crosshair/line position on the non-coplanar/scout image with respect to the axial slice location. Inaccurate placement of reference lines or crosshairs have potential risk of misdiagnosis or mistreatment due to unintended shifts in the display of anatomical locations.
Recommended Action
Per FDA guidance
AGFA issued Urgent: Mandatory Correction Important Information on 9/10/24. Letter states reason for recall, health risk and action to take: AGFA HealthCare will provide the software corrections for the affected versions. A patch is available for each of the following XERO Viewer version streams: - 8.4.x - 8.3.x - 8.2.x - 8.1.4.x - 8.1.2.x For versions of XERO Viewer prior to 8.1.2, the issue can be prevented from happening at your site by: - Using the XERO Viewer Extended Tools component (Xtend), if enabled. - Using the Enterprise Imaging Desktops viewer. - There is an option to disable the features affected by this issue. This can be configured by your administrator or contact AGFA Support. Our Support organization representative will contact all customers on any of these versions and coordinate the correction activity. The patch installation will not require any downtime. We request that you complete and return the attached mandatory feedback form. Please direct questions or concerns to your AGFA HealthCare Customer Support, and please reference PRB0762354. AGFA HealthCare Customer Support: 1.866.599.3868
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026