Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 22831 |
| Brand Name: | Philips MultiDiagnost Eleva |
| Model: | MultiDiagnost Eleva 708032, MultiDiagnost Eleva with Flat Detector 708034, MultiDiagnost Eleva with Flat Detector 708038 |
| 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 Nederland BV |
| Issue: | The manufacturer has become aware that the fixation of the upper and lower tilt actuator of the MD-Eleva system might break off and the table will start to rotate from 0 to + 90 / - 90 degrees with high speed if the point of gravity of the table is beyond its rotation point. This rotating movement can not be stopped by the user, which potentially could lead to the patient falling off the table. |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 18/4/2018 |
