Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 24042 |
| Brand Name: | Philips MR Systems Intera, Enterprise, Achieva, Achieva XT, Achieva Conversion, Panaorama HFO, Ingenia, Smartpath to dStream, Multiva, Prodiva, MR-OR, MR-RT, MR-Linac, MR-MarlinIngenia Series |
| Model: | Intera, Omniva, Enterprise, Achieva, Achieva XR, Achieva Conversion, Panorama HFO, Ingenia, SmartPath to dStream, Multiva, Prodiva, MR-OR, MR-RT, MR-Linac, MR-Marlin systems |
| 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: | In very rare cases, due to external influences (hospital facility maintenance, water leakage, degradation of speaker fixation) during the lifetime of the MR system, the ceiling speaker(s) could fall from their position and be pulled to the MR system by the magnetic field. |
| Recall action type: | Correction |
| Recall action: | |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 3/1/2019 |
