Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 28193 |
| Brand Name: | CombiDiagnost R90 |
| Model: | Model number - 709030 - software - R1.0, R1.1 |
| 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: | The manufacturer has become aware of a software issue, where the kV and mA values are not locked but change when the collimator shutter position is changed directly after the Lock-In command. This software issue leads to an over or under exposed image. However, if the user stops and restarts fluoroscopy, then the Lock-In works as specified. |
| Recall action type: | Correction |
| Recall action: | Software to be upgraded |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 16/8/2021 |
