Company:Siemens Medical Solutions USA, Inc.
Date of Enforcement Report: 11/4/2015
Class lI:
PRODUCT
CIOS ALPHA; image intensified fluoroscopic x-ray system
Recall Number Z-0118-20166
REASON
patient procedure interruption due to a potential system failure
RECALLING FIRM/MANUFACTURER
Siemens Medical Solutions USA, Inc, Malvern, PA on 8/7/2015 Voluntary: Firm Initiated recall is ongoing
VOLUME OF PRODUCT IN COMMERCE
44
DISTRIBUTION
Nationwide
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