Philips Medical Systems Technologies Ltd.: Device Recall
Recall #Z-0497-2025 · 10/10/2024
Recall Details
- Recall Number
- Z-0497-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Philips Medical Systems Technologies Ltd.
- Status
- Ongoing
- Date Initiated
- 10/10/2024
- Location
- Haifa, N/A, Israel
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2439 systems
Reason for Recall
A software issue affecting Philips Vue PACS may cause incorrect ischemic map and table value calculations when using the export function in the Perfusion Application for a Siemens CT perfusion study, resulting in misdiagnosis due to incorrect ischemic map and table values.
Product Description
Vue PACS Diagnostic Viewer with Vue PACS client 12.1.5 to 12.2.8.454 software Model Number: 1149418 Intended use is to provide completely scalable local and wide area PACS (Picture Archiving and Communication System) solutions for hospital and related institutions/sites.
Distribution Pattern
US Nationwide and Worldwide Distribution Foreign: Country Argentina Australia Austria Belgium Brazil Chile China Colombia Denmark Finland France Germany Gibraltar Greece Guernsey Holy See (Vatican City State) Hong Kong Hungary Indonesia Ireland Israel Italy Japan Jersey Jordan Lebanon Malaysia Mexico Netherlands New Zealand Norway Oman Panama Philippines Poland Portugal Romania Saudi Arabia Serbia Slovenia Spain Sweden Switzerland Taiwan Thailand United Kingdom