Retiro De Equipo (Recall) de BrightView SPECT, BrightView X and BrightView XCT Software Software Versions: V1.2.3 (Brightview SPECT and X) / V2.5.3 (Brightview XCT)

Recall

RC-2014-RN-01224-1

Class I

2014-11-27

Australia

DHTGA

https://apps.tga.gov.au/Prod/sara/arn-detail.aspx?k=RC-2014-RN-01224-1

The following anomalies may result in unintended patient contact with a detector or gantry:following a cardiac scan and when using smartstep to set-up the camera for a relative 180 procedure, it is possible for detector 1 to collide with the head holder when moving from the position at which the flat panel is deployed. this was identified during in-house testing on a brightview xct system onlyduring a patient spect lung acquisition, the gantry rotation may move from the 45 degree to the 90 degree position. in the middle of a clinical scan acquisition, the detector heads moved away from the patient (centre of rotation) in an uncommanded motion and subsequently the gantry unexpectedly rotated to the 240 degree position. the movement from 90 degree to the 240 degree may take 7 secondsat the completion of a thyroid procedure the operator executed the pinhole pre-programed motion and noticed a change in the sequence of motions between the imaging pallet and the detector radius.

Philips is advising the customer/user to perform the work-around identified in the customer communication prior to the implementation of the permanent correction, to avoid contact between the detector and the head holder. Further, customers are advised to monitor the patient during all system motions and to know locations of the multiple E-Stop button(s) to halt all system motions, if required. The correction will consist of the installation of BrightView Family software version 1.2.4/2.5.4.