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U.S. Department of Health and Human Services

Class 2 Device Recall Luminos Agile Max

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  Class 2 Device Recall Luminos Agile Max see related information
Date Initiated by Firm January 08, 2020
Create Date August 05, 2020
Recall Status1 Open3, Classified
Recall Number Z-2756-2020
Recall Event ID 85999
510(K)Number K173639  
Product Classification System, x-ray, fluoroscopic, image-intensified - Product Code JAA
Product SIEMENS Healthineers Luminos Agile Max
Model: 10762472 - Product Usage: is a device intended to visualize anatomical structures by converting an X-ray pattern into a visible image.
Code Information Serial Numbers: 61203 61751 61085 61755 61858 61786 61795 61034 61127 61602 61212 61053 61194 61699 61757 61752 61200 61738 61799 61875 61603 61624 61885 61848 61243 61606 61682 61087 61888 61052 61889 61226 61854 61079 61218 61110 61137 61123 61763 61621 61622 61623 61788 61798 61837 61892 61193 61700 61743 61652 61229 61045 61838 61239 61632 61190 61013 61659 61102 61724 61063 61054 61784 61213 61651 61056 61088 61146 61681 61678 61873 61720 61716 61027 61021 61145 61824 61050 61210 61211 61240 61227 61185 61779 61140 61181 61061 61158 61242 61074 61209 61075 61686 61094 61032 61769 61608 61711 61869 61169 61223 61083 61234 61660 61661 61849 61143 61670 61616 61723 61754 61684 61249 61691 61130 61668 61806 61717 61174 61740 61722 61777 61126 61255 61855 61015 61183 61046 61804 61731 61748 61845 61822 61863 61719 61829 61162 61125 61156 61713 61196 61028 61076 61787 61825 61683 61081 61758 61609 61618 61744 61111 61248 61704 61890 61656 61663 61636 61827 61159 61114 61635 61132 61112 61118 61253 61664 61177 61733 61040 61641 61646 61151 61238 61673 61831 61221 61832 61638 61207 61133 61695 61671 61631 61201 61833 61865 61148 61128 61625 61815 61236 61828 61810 61172 61839 61116 61168 61175 61662 61048 61171 61060 61649 61768 61042 61115 61813 61188 61191 61206 61708 61665 61746 61747 61862 61230 61667 61881 61113 61771 61044 61147 61096 61617 61035 61861 61134 61033 61066 61155 61224 61876 61847 61157 61634 61844 61178 61882 61883 61065 61801 61841 61874 61068 61069 61880 61674 61680 61830 61776 61736 61761 61186 61766 61783 61756 61772 61797 61793 61843 61614 61250 61251 61868 61219 61803 61753 61856 61107 61152 61093 61091 61014 61025 61208 61791 61256 61654 61173 61154 61189 61142 61165 61842 61734 61759 61718 61878 61840 61043 61781 61785 61601 61687 61647 61895 61897 61036 61669 61038 61739 61679 61857 61049 61022 61037 61098 61792 61215 61707 61153 61715 61894 61611 61120 61150 61633 61029 61884 61657 61887 61072 61812 61879 61819 61187 61693 61800 61727 61696 61062 61820 61821 61725 61139 61141 61775 61080 61217 61689 61030 61778 61627 61018 61790 61222 61078 61086 61216 61195 61809 61039 61252 61860 61750 61721 61811 61807 61728 61202 61064 61163 61859 61835 61891 61077 61228 61871 61605 61767 61836 61826 61851 61630 61850 61896 61192 61690 61084 61823 61620 61749 61714 61770 61047 61121 61220 61729 61712 61225 61735 61802 61103 61628 61109 61198 61818 61626 61877 61247 61180 61644 61615 61244 61643 61705 61697 61742 61031 61097 61164 61166 61237 61245 61610 61612 61629 61655 61666 61672 61675 61676 61773 61780 61814 61101 61160 61233 61741 61041 61055 61782 61057 61059 61067 61099 61100 61106 61258 61653 61852 61870 61702 61017 61730 61765 61129 61246 61184 61604 61179 61677 61703 61774 61698 61864 61254 61073 61789 61131 61205 61872 61119 61637 61764 61051 61138 61866 61834 61619 61760 61122 61853 61816 61893 61613 
Recalling Firm/
Manufacturer
Siemens Medical Solutions USA, Inc
40 Liberty Blvd
Malvern PA 19355
For Additional Information Contact SAME
610-219-4834
Manufacturer Reason
for Recall
Two software issues (1) Using the override function in case of blocked system movements affecting Luminos dRF Max, Luminos Agile Max and Uroskop Omnia Max systems may cause collision of the system under operator control with obstacles or persons .(2) Incorrectly assigned image affecting Ysio Max, Luminos dRF Max and Luminos Agile Max systems with detector MAX Static causing incorrect base for diagnosis
FDA Determined
Cause 2
Device Design
Action Siemens Medical Solutions USA, Inc. has initiated a Customer Safety Advisory Notice to all affected customers via XP028/19/S January 2020. Additionally, a solution to eliminate the root cause of this problem is being distributed via XP008/20/S March 2020. Following the corrective action, the cause is eliminated and a recurrence of the fault is prevented. New corrective software VE10Y became available June 22, 2020, and it is being distributed via an Update Instruction XP008/20/S. This update fixes the initial reported issue and the sporadic image loss issue noted by customers who had already installed VE10W (XP029/19/S). The original Customer Safety Advisory Notice (XP028/19/S) and the information letter distributed in March 2020 remain applicable. This resolution will be provided free of charge. Your local Siemens Healthineers Service organization will contact you to arrange a date to perform this corrective action . Questions contact the service organization for an earlier appointment at 1-800-888-7436
Quantity in Commerce 477 units
Distribution US Nationwide distribution.
Total Product Life Cycle TPLC 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 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
510(K) Database 510(K)s with Product Code = JAA and Original Applicant = Siemens Medical Solutions, Inc
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