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YSIO MAX (2015-04-10)

Starting date:
April 10, 2015
Posting date:
April 30, 2015
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type III
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-53183

Recalled Products

A. YSIO MAX

Reason

Images might be lost and corresponding acquisitions have to be repeated under the following circumstances: 
-during an image recovery process on systems with portable detectors (Max WI-D, Max Mini) the connection of the portable detector is sporadically not re-established.
-if either the "undo" button on the rad subtask card or the "previous series" button on the image subtask card are pressed during image readout.
-sporadically, during an automatic or a manual RIS update. This may cause the deletion of the currently used study and all acquired images within this study.

Affected products

A. YSIO MAX

Lot or serial number

SN 24102

Model or catalog number

10762470

Companies
Manufacturer
Siemens Ag
Wittelsbacherplatz 2
Muenchen
80333
GERMANY