Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 28703 |
| Brand Name: | CombiDiagnost R90 |
| Model: | Multiple model numbers |
| 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: | Hamburg DXR |
| Model: | Multiple model numbers |
| 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: | Bucky Diagnost- TC/TH/VE/VT/CS III/ FS/TH2/TF/VS |
| Model: | Multiple model numbers |
| 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 an anomaly with our Philips DigitalDiagnost 1.x, 2.x, 3.x, 4.x, BuckyDiagnost, EasyDiagnost, TraumaDiagnost, ProGrade, ProxiDiagnost N90, and CombiDiagnost R90 Radiography Systems (that use ceiling suspension). If a user, while cleaning or disinfecting the control handle of the ceiling suspension, uses excessive liquid or if liquid is sprayed directly on the system, it is possible for liquid to enter around the edges of the button onto the movement activation switch (6) creating a short circuit and activation of the brake release. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 9/12/2021 |
