Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 23853 |
| Brand Name: | CombiDiagnost R90 |
| Model: | All CombiDiagnost systems with software version 1.0.0, 1.0.1 and 1.0.2 |
| 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 DMC GmbH |
| Issue: | Due to a software bug, the mA values are not locked, but increase when the operator restarts pulsed fluoroscopy several times after activation of the lock-in function. As a result, the patient received an increased radiation dose |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 15/11/2018 |
