Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:20940
Brand Name: X-ray System Angiographic
Model:
Affected: Prestige 2, Prestilix, Prestige VH, Prestige SI, RFX/SFX, Legacy and Precision 500D, ADVANTX and Innova 2000 systems
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 SCS
Issue:There have been reported incidents of a Distar CRT monitor that has fallen off the monitor suspension related to product ageing.
Recall action type:Correction
Recall action:Product to be modified
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:16/12/2016
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