Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 28555 |
| Brand Name: | CombiDiagnost R90 (MDR) |
| Model: | 709031 |
| 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 |
| Brand Name: | CombiDiagnost R90 |
| Model: | 709130 |
| 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 |
| Brand Name: | Digital Diagnost C90 MDR |
| Model: | 712034, 712035 |
| 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 identified that the CombiDiagnost R90 and DigitalDiagnost C90 can be equipped with an additional X-ray tube assembly at a ceiling suspension. When the control grip of the ceiling suspension is cleaned with disinfectants and disinfectant remains on the control grip, it can create a false activation of the touch sensor that enables brake release. If the brake is released, there is a potential for unintended movement. This issue will not occur once the disinfectant on the control grip dries. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 5/11/2021 |
