Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 28804 |
| Brand Name: | MRI system, full-body, superconducting magnet |
| Model: | GEHC Magnetic Resonance (MR) systems |
| Affected: | |
| Software version: | |
| Recalling Organisation: | GE Healthcare Limited Level 7, Vero Centre 48 Shortland St Auckland 1010 |
| Contact Information: | 0800 659 465 |
| Manufacturer: | GE Medical Systems LLC |
| Issue: | The manufaturer has identified that the magnetic Resonance (MR) systems could potentially have a cryogen ventilation system that does not meet the venting requirements. |
| Recall action type: | Correction |
| Recall action: | Manufacturer to issue advice regarding use |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 11/1/2022 |
