Database updated: 27 October 2026

Safety Information

Medsafe Online Recall Database

Detail of Recall

Type of Product:Device
Medsafe Reference:20023
Brand Name:Siemens e.cam and all Symbia systems with foresight detectors
Model:
Affected:10151532, 8717733, 10275009, 10275010, 10275879, 8717741, 10275008, 10275007, 10764804, 10764803, 10764801, 10764802, 10910501, 10151531 with foresight detectors
Software version:
Recalling Organisation:Siemens Healthcare (NZ) Ltd
Millennium Centre, Part Level 2, Building A
600 Great South Road
Ellerslie
AUCKLAND 1051
Contact Information:0800 310 300
Manufacturer:Siemens Medical Solutions USA Inc
Issue:Affected systems performing gated or dynamic acquisitions may lose some detector time-information this may result in framing of the image data and the calculated ejection fraction values may be lower. Misdiagnosis may be possible.
The resulting risk is that the framing of the image data and the calculated ejection fractions values may be lower.
Recall action type:Correction
Recall action:Software to be upgraded
Level of recall:Hospital/Pharmacy/Laboratory
Date Commenced:12/4/2016
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