Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:15570
Brand Name:GE Vivid E9 Ultrasound System
Model:
Affected:
Software version:112.1.0, 112.1.1, 112.1.3
Recalling Organisation:GE Healthcare Limited
Level 7, Vero Centre
48 Shortland St
Auckland 1010
Contact Information:0800 659 465
Manufacturer:GE Vingmed Ultrasound AS
Issue:Keyboard response time on the system may increase, and possibly eventualy result in the system being locked. This only occurs when used together with a GE transesophageal echocardiography probe for certain types of procedures.
GE will correct all affected systems and the FMI is expected to be released in Nov 2013 and all sites completed by Feb 2014.
Recall action type:Correction
Recall action:Software to be upgraded
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:24/10/2013
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