Mavig Monitor suspension arms manufactured before January 2009 (used with x-ray fluoroscopic imaging systems) Installed on INNOVA 2100, 3100 fluoroscopic imaging systems. 의 리콜

Recall

RC-2016-RN-00003-2

Class II

2016-01-04

Australia

DHTGA

https://apps.tga.gov.au/Prod/sara/arn-detail.aspx?k=RC-2016-RN-00003-2

Ge healthcare has become aware of a reported incident in which a mavig suspension arm with monitor assembly fell to the floor. the failure of spring arm rotating plate will lead to a sudden fall of the spring arm with monitors of mavig suspension. such a fall could result in bodily harm to a person. there have been no injuries reported as a result of this issue.

GE Healthcare will correct all affected products. In the interim, users are advised to avoid placing the monitor over a patient, or user or other auxiliary personnel. If users observe any unusual movement or looseness of the Mavig Monitor suspension, they are advised to contact their GE Healthcare representative and follow the precautions below before continuing to use the monitor(s): 1) Position the monitor suspension in the most frequently used position and limit further movement as much as possible. 2) Clearly inform (e.g. through signage and verbal instructions) the users and other auxiliary personnel who may come in contact with the system to not move the monitor suspension once in position. GE Healthcare will send a representative to inspect the system. This action has been closed-out on 04/05/2017.