| Type of Product |
Medical Device |
| TGA Recall Reference |
RC-2013-RN-01118-1 |
| Product Name/Description |
E.cam and Symbia E systems (diagnostic nuclear medicine imaging system)
All Siemens e.cam 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 |
|
| Reason/Issue |
The manufacturer has received reports of loose bolts on system detectors for Symbia E and e.cam, 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 |