Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 25974 |
| Brand Name: | Hamburg DXR |
| Model: | All TraumaDiagnost |
| 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 Trauma arm is connected to the telescopic column of the ceiling suspension by a shaft, which is fixed to a supporting block. If the shaft breaks, the trauma arm can fall down. There is the potential for a serious injury if one of the following occurs: Fatigue fracture (crack) of the shaft Crack increases during lifetime without being noticed by the operator or service engineer (unusual angle of Trauma arm) Shaft breaks Person located nearby falling trauma arm |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 28/4/2020 |
