Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 30293 |
| Brand Name: | PMS Nederland MR Systems (MDR) |
| Model: | Philips Ingenia Elition X, Ingenia Elition S and MR 7700 |
| 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 |
| Brand Name: | Ingenia, Achieva Series |
| Model: | Philips Ingenia Elition X, Ingenia Elition S and MR 7700 |
| 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 identified an issue where a specific component failure in the Gradient Coil of where the Affected 3T MR Systems may act as a heat source, with a potential to produce smoke and/or fire. If the component failure occurs, the user may observe the following: * Severe image quality issues (image artifacts caused by electrical disturbances) * Smoke and/or fire. |
| Recall action type: | Correction |
| Recall action: | Product to be modified |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 17/7/2023 |
