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U.S. Department of Health and Human Services

Class 2 Device Recall Siemens Artis Q ceiling

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 Class 2 Device Recall Siemens Artis Q ceilingsee related information
Date Initiated by FirmJune 06, 2019
Create DateJune 28, 2019
Recall Status1 Terminated 3 on February 09, 2021
Recall NumberZ-1899-2019
Recall Event ID 83082
510(K)NumberK181407 
Product Classification Interventional fluoroscopic x-ray system - Product Code OWB
ProductSiemens Artis Q ceiling--Interventional Fluoroscopic X-Ray System Model Number: 10848281
Code Information Serial Numbers: 109007 109057 109028 109027 109011 109021 109009 109010 109072 109075 109071 109041 109039 109032 109020 109036 109048 109088 109101 109040 109034 109031 109043 109067 109068 109093 109080 109179 109134 109133 109496 109076 109105 109104 109107 109084 109060 109164 109167 109135 109119 109090 109096 109091 109146 109102 109092 109189 109129 109143 109183 109606 109144 109171 109155 109217 109159 109172 109211 109169 109229 109166 109388 109350 109332 109210 109309 109203 109369 109300 109202 109401 109302 109346 109429 109214 109301 109311 109320 109330 109349 109373 109361 109231 109379 109331 109432 109434 109324 109417 109327 109344 109367 109435 109352 109380 109515 109461 109386 109365 109415 109366 109412 109383 109493 109518 109445 109437 109558 109526 109458 109424 109456 109451 109463 109467 109598 109484 109536 109538 109500 109501 109592 109527 109569 109627 109599 109591 109613 109610 109628 
FEI Number 2240869
Recalling Firm/
Manufacturer		 Siemens Medical Solutions USA, Inc
40 Liberty Blvd
Malvern PA 19355-1418
For Additional Information ContactSAME
610-219-4834
Manufacturer Reason
for Recall		Artis Zee, Artis Q, Artis Pheno or Artis Icono systems equipped with a DCS Extended or DCS Movable, the potential exists for individual screws of the screwed connection joining the pivot bearing to the ceiling-mounted support to work loose or snap off, can result in severe injuries to patients and operating personnel
FDA Determined
Cause 2		Device Design
ActionSiemens issued letter dated 6/6/19 advising of the problem, health risk and action to take: .Siemens is implementing a corrective action to all potentially affected users via Update Instruction AX023/18/S. Siemens Service organization will replace the screwed connection of the ceiling support according to specifications / instructions. In the event the bolt connection cannot be replaced due to technical conditions, the complete bearing will be replaced.
Quantity in Commerce131
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 = OWB
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