Z-0055-2025Class II

Enterprise Imaging XERO Viewer- software application used for reference and diagnostic viewing of...

Name: Z-0055-2025 Enterprise Imaging XERO Viewer- software application used for reference and diagnostic viewing of...
Creator: Agfa Healthcare NV
Published: 2024-09-06
License: https://open.fda.gov/license/

AGFA Healthcare Corp. / initiated 2024-09-06 / Open, Classified / root cause: software

FDA source

Agfa Healthcare NV began a recall of Enterprise Imaging XERO Viewer- software application used for reference and diagnostic viewing of multispecialty medical imaging and non-imaging data... on 2024-09-06. FDA classified it as Class II and gives the reason as "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...". As of 2026-09-10, the recall status on record is Open, Classified, and MDM tags the root cause as software.

Recall record

Recall number: Z-0055-2025
Classification: Class II
Status: Open, Classified
Initiated: 2024-09-06
Posted: 2024-10-10
Recalling firm: AGFA Healthcare Corp.
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)
Product code: LLZ System, Image Processing, Radiological
Reason for recall: 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.
Root cause tag: software
FDA root cause: Software design
Action: 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
Quantity in commerce: 801 units
Distribution: US Nationwide distribution. Foreign: Argentina, Australia, Belgium, Chile, Canada, Colombia, Croatia, Cura¿ao, Cyprus, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, Estonia, Georgia, Greece, Hong Kong, Iceland, Ireland, Italy, Jordan, Kazakhstan, Kenya, Kuwait, Lebanon, Luxembourg, Mexico, Netherlands, Nicaragua, Norway, Oman, Pakistan, Peru, Poland, Romania, Russian Federation, San Marino, Saudi Arabia, Singapore, Slovenia, South Africa, Spain, Sweden, Tanzania, Tunisia, United Arab Emirates, United Kingdom
Product codes and lots: 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

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-0055-2025
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-0055-2025	Class II	Ongoing	Voluntary: Firm initiated	2024-10-16	2024-10-10

Product code LLZ

K170434Class IIEnterprise Imaging XERO Viewer 8.1Agfa Healthcare N.V. / cleared 2017-07-03

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)