Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 20403 |
| Brand Name: | Philips Multidiagnost Eleva and Multidiagnost Eleva with Flat Detector |
| Model: | MultiDiagnost Eleva, MultiDiagnost Eleva with Flat Detector |
| Affected: | 708032, 708034, 708036, 708038 |
| 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 Nederland BV |
| Issue: | The two bolts that attach the clamping plate to the lateral shaft may break. This may cause the C-arm to float freely. Depending on the orientation of the free-floating C-arm and any other forces applied to it the C-arm could move laterally forward, slide out of its bearings and then possibly sag. |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 15/7/2016 |
