Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Vue PACS Diagnostic Viewer with Vue PACS client 12.1.5 to Recalled by Philips Medical Systems Technologies Ltd. Due to A software issue affecting Philips Vue PACS may...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Philips Medical Systems Technologies Ltd. directly.
Affected Products
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.
Quantity: 2439 systems
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips Medical Systems Technologies Ltd.
Philips Medical Systems Technologies Ltd. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report