Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 29060 |
| Brand Name: | Hemodynamic Application |
| Model: | Philips Hemodynamic Application R1.2.2 and R1.2.3 |
| Affected: | |
| Software version: | |
| Recalling Organisation: | Philips New Zealand Commercial Limited Level 3 123 Carlton Gore Road Newmarket AUCKLAND 1023 |
| Contact Information: | 0800 251 400 |
| Manufacturer: | Philips Medical Systems Nederland BV |
| Issue: | The manufacturer has identified that when a Neonatal patient is admitted in the Philips Hemodynamic Application, the Non-Invasive Blood Pressure is not set to Neonatal on the Philips Xperflex Cardio FC2010 patient monitor. The Philips Hemodynamic Application will indicate 'Neonatal' on the Non-Invasive Blood Pressure (NIBP) field displayed on the User Interphase (UI) in the control and exam room, but the FC2010 NIPB will be set in Adult mode. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 3/3/2022 |
