MalfunctionMWI
Hemodynamic Systems
Received Jul 31, 2026 · Event occurred Jul 8, 2026
Report 1051786-2026-100051 · MDR key 50100639
Device
Generic name
Cardiac Electrophysiology, Diagnostics, And Monitoring Devices
Manufacturer
Invivo, A Division Of Philips Medical SystemsModel number
722450Catalog number
722450
Product problems
- Incorrect Measurement
Patient
Unknown
- No Clinical Signs, Symptoms or Conditions
Narrative
Description of Event or Problem
Philips received a complaint on the Hemodynamic Systems indicating the venus blood pressure is not accurate. The device was in use on patient at time of event, there was no adverse event reported.
Additional Manufacturer Narrative
Philips is in the process of obtaining additional information concerning this event and the complaint is still under investigation. A final report will be submitted once the investigation is complete.