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U.S. Department of Health and Human Services

Class 2 Device Recall MULTISTAR POLYDOROS XRay System

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 Class 2 Device Recall MULTISTAR POLYDOROS XRay Systemsee related information
Date Initiated by FirmAugust 11, 2008
Date PostedNovember 04, 2008
Recall Status1 Terminated 3 on December 21, 2012
Recall NumberZ-0142-2009
Recall Event ID 49426
510(K)NumberK930635 
Product Classification angiographic x-ray system - Product Code IZI
ProductMULTISTAR POLYDOROS X-Ray System, Model number 2845001
Code Information Model number 2845001 - Serial numbers: 1014 and 1027 
Recalling Firm/
Manufacturer
Siemens Medical Solutions USA, Inc
51 Valley Stream Pkwy
Malvern PA 19355
Manufacturer Reason
for Recall
Unintended movement of the system table and/or C arm.
FDA Determined
Cause 2
Software design
ActionSiemens Medical Solutions issued a letter to consignees on 8/11/2008 to inform them of the problem and a workaround should the issue occur prior to software revision.
Quantity in Commerce2 units
DistributionNationwide.
Total Product Life CycleTPLC Device Report

1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database510(K)s with Product Code = IZI
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