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Type of Product Medical Device
TGA Recall Reference RC-2013-RN-01118-1
Product Name/Description and Symbia E systems (diagnostic nuclear medicine imaging system)

All Siemens and Symbia E systems affected

Siemens Reference Number: MI017/13/S

ARTG Number: 186317
Recall Action Level Hospital
Recall Action Classification Class II
Recall Action Commencement Date 30/10/2013
Responsible Entity Siemens Ltd
Reason/Issue The manufacturer has received reports of loose bolts on system detectors for Symbia E and, which secure the detectors to the yoke.
Recall Action Recall for Product Correction
Recall Action Instructions Siemens is advising users that all affected units will be inspected for loose screws and corrected if required. Affected units can continue to be used.
Contact Information 1800 310 300 - Siemens Technical Support Centre