Jul

2018

Recall – X-Ray System

Company: Siemens Medical Solutions USA, Inc
Date of Enforcement Report 7/4/2018
Class II:

PRODUCT
Artis Q ceiling, Material no. 10848281, for angiography and whole body radiographic/fluoroscopic procedures. Recall Number: Z-2304-2018

REASON
After the Large Display returns from power save mode, it may not show an image, and stay black without showing an error message although X-ray is still possible. The problem does not occur during an ongoing procedure. If the problem occurs, the system cannot be operated normally. It may be necessary to cancel or restart the treatment or transfer the patient to an alternate or another system..

RECALLING FIRM/MANUFACTURER
Siemens Medical Solutions USA, Inc, Malvern, PA on 5/1/2018. Voluntary: Firm Initiated recall is ongoing.

VOLUME OF PRODUCT IN COMMERCE
5

DISTRIBUTION
Nationwide and Internationally

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Recall – X-Ray System

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