Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 20379 |
| Brand Name: | Philips Dura Diagnost |
| Model: | 451220108521, 459800968541 |
| 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 Healthcare (Suzhou) Co Ltd |
| Issue: | DuraDiagnost systems provide an audible exposure termination signal (Beep) through the speaker integrated into the monitor. However, buttons or keys on the monitor allow the user to turn the volume setting down to "0", in which case the beep will not be heard at the conclusion of an exposure |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 12/7/2016 |
