Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:29109
Brand Name:MRI system, full-body, superconducting magnet
Model:All GE MRI 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:As a follow up to the manufacturer's Urgent Medical Device Correction Letter, they are now providing a Magnet Deinstallation Manual that includes specific safety requirements and specifications for the safe de-installation of the GE Healthcare MR System
Recall action type:Correction
Recall action:Manufacturer to issue advice regarding use
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:11/10/2022
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