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U.S. Department of Health and Human Services

Class 2 Device Recall SOMATOM Sensation 16

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 Class 2 Device Recall SOMATOM Sensation 16see related information
Date Initiated by FirmSeptember 28, 2004
Date PostedNovember 03, 2004
Recall Status1 Terminated 3 on September 04, 2008
Recall NumberZ-0158-05
Recall Event ID 30173
510(K)NumberK013522 
Product Classification System, X-Ray, Tomography, Computed - Product Code JAK
ProductSOMATOM CT System Sensation 16, Computed Tomography X-Ray, Model Number 73 93 114
Code Information Serial Numbers: 50008, 50013, 50014, 50022, 50025, 50026, 50027, 50029, 50034, 50036, 50037, 50040, 50042, 50044, 50048, 50050, 50054, 50058, 50062, 50066, 50073, 50075, 50079, 50081, 50085, 50086, 50089, 50093, 50096, 50097, 50100, 50105, 50106, 50110, 50113, 50123, 50124, 50131, 50134, 50138, 50139, 50141, 50142, 50146, 50152, 50154, 50156, 50158, 50162, 50165, 50166, 50168, 50174, 50175, 50178, 50181, 50183, 50186, 50190, 50192, 50193, 50194, 50202, 50203, 50205, 50212, 50219, 50222, 50224, 50226, 50234, 50238, 50245, 50249, 50250, 50255, 50258, 50262, 50263, 50266, 50273, 50274, 50278, 50283, 50285, 50288, 50293, 50300, 50308, 50310, 50316, 50317, 50325, 50327, 50332, 50334, 50340, 50343, 50351, 50356, 50365, 50374, 50379, 50380, 50391, 50392, 50394, 50394, 50396, 50409, 50412, 50416, 50421, 50429, 50433, 50435, 50452, 50454, 50455, 50458, 50459, 50461, 50462, 50465, 50466, 50467, 50471, 50472, 50473, 50479, 50482, 50483, 50488, 50490, 50491, 50494, 50497, 50501, 50512, 50525, 50530, 50534, 50535, 50540, 50543, 50549, 50550, 50555, 50556, 50557, 50560, 50561, 50564, 50568, 50570, 50573, 50575, 50576, 50577, 50579, 50580, 50582, 50585, 50588, 50590, 50591, 50595, 50597, 50600, 50609, 50610, 50611, 50615, 50621, 50622, 50626, 50627, 50628, 50631, 50632, 50636, 50639, 50640, 50643, 50644, 50545, 50650, 50651, 50653, 50665, 50668, 50669, 50672, 50674, 50682, 50683, 50685, 50686, and 50999.
Recalling Firm/
Manufacturer		 Siemens Medical Solutions USA, Inc
51 Valley Stream Pkwy
Malvern PA 19355-1406
For Additional Information ContactRoland Richter,
610-448-1777
Manufacturer Reason
for Recall		Calcium Scoring feature on this devices is not closing properly after patient's exams.
FDA Determined
Cause 2		Other
ActionThe recalling firm issued a Customer Safety Advisory with Update Instructions, CT036/04/S and CN048.04/2 to their affected customers. The letter informed the customers of the potential issue and provided instructions to avoid the problem while using this feature. A software upgrade is being developed to corect this issue.
Quantity in Commerce199 units
DistributionThe product was shipped to medical facilities nationwide and government account in IL.
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 = JAK
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