Database updated: 27 October 2026
Safety Information
Medsafe Online Recall Database
Detail of Recall
| Type of Product: | Device |
| Medsafe Reference: | 29012 |
| Brand Name: | MRI system, full-body, superconducting magnet |
| Model: | GE Signa 1.5T TwinSpeed, 1.5T Signa Excite HD, 3.0T Signa Excite HD, GE Signa 3.0T with Excite, GE 1.5T Signa HDx, 3.0T Signa HDx, GE 1.5T HDxt, GE 3.0T Signa HDxt, 1.5T Signa HDxt Mobile Magnetic Resonance System's |
| 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: | As a follow up the manufacturer are providing a revised service manuals that include the Finalization Step. To access the revised manuals for the following affected MR systems, please follow the instructions to download the latest version of the service manuals. |
| Recall action type: | Correction |
| Recall action: | Instructions for use to be updated |
| Level of recall: | Hospital/Pharmacy/Laboratory |
| Date Commenced: | 23/2/2022 |
