Device evidence

device-recall:cfres:207659

Philips Interventional Hemodynamic Application R.1.2X, R.1.3.0, R1.2.1. Software that enables invasive investigation of cardiac and vascular diseases.

Official recall number

Z-1926-2024

Evidence summary

Product code: MWI
Recall status: Open, Classified
Event initiated: May 02, 2024
Root cause: Component design/selection
Source snapshot: 5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product: Z-1926-2024