Events

Recall of BrightView SPECT, BrightView X and BrightView XCT Software Software Versions: V1.2.3 (Brightview SPECT and X) / V2.5.3 (Brightview XCT)

According to Department of Health, Therapeutic Goods Administration, this recall involved a device in Australia that was produced by Philips Electronics Australia Ltd.

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    RC-2014-RN-01224-1
  • Event Risk Class
    Class I
  • Event Initiated Date
    2014-11-27
  • Event Country
    Australia
  • Event Source
    DHTGA
  • Event Source URL
    https://apps.tga.gov.au/Prod/sara/arn-detail.aspx?k=RC-2014-RN-01224-1
  • Notes / Alerts
    Australian data is current through July 2018. All of the data comes from the Australian Therapeutic Goods Administration, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Australia.
  • Extra notes in the data
  • Reason
    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.
  • Action
    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.

Device

BrightView SPECT, BrightView X and BrightView XCT Software Software Versions: V1.2.3 (Brightview ...

Manufacturer

Philips Electronics Australia Ltd
  • Manufacturer Parent Company (2017)
    Philips
  • Source
    DHTGA