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Type of Product Medical Device
TGA Recall Reference RC-2013-RN-00439-1
Product Name/Description BrightView SPECT (single photon emission computed tomography system)

ARTG Number: 117642
Recall Action Level Hospital
Recall Action Classification Class I
Recall Action Commencement Date 13/05/2013
Responsible Entity Philips Electronics Australia Ltd
Reason/Issue A failure of the mechanical assembly may result in unintended motion of the detector.
Recall Action Recall for Product Correction
Recall Action Instructions Phillips Healthcare will conduct inspections of all systems and carry out a field correction if required.

Phillips has advised that if the system passes inspection it is safe to continue using the device.
Contact Information 1800 251 400 - Philips Customer Care Centre