Events

Rappel de ACUSON Aspen Diagnostic Ultrasound System

Selon U.S. Food and Drug Administration, ce/cet/cette rappel concerne un dispositif en/au/aux/à United States qui a été fabriqué par Siemens Medical Solutions USA, Inc..

Qu'est-ce que c'est?

Une correction ou un retrait opéré par un fabricant afin de répondre à un problème causé par un dispositif médical. Les rappels surviennent lorsqu'un dispositif médical est défectueux, lorsqu'il pourrait poser un risque pour la santé, ou les deux à la fois.

En savoir plus sur les données ici
  • Type d'événement
    Recall
  • ID de l'événement
    45411
  • Classe de risque de l'événement
    Class 2
  • Numéro de l'événement
    Z-1107-2004
  • Date de mise en oeuvre de l'événement
    2007-09-18
  • Date de publication de l'événement
    2008-02-15
  • Statut de l'événement
    Terminated
  • Pays de l'événement
    United States
  • Date de fin de l'événement
    2011-04-21
  • Source de l'événement
    USFDA
  • URL de la source de l'événement
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=65394
  • Notes / Alertes
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Notes supplémentaires dans les données
    Autoperfusion Software - Product Code IYN
  • Cause
    Software error: error affects all aspen customer systems using the pal video standard configuration and have a perspective pc installed. this can lead to a measurement error under this specific condition: on secondary capture images/clips stored from within any perspective advanced display option (specifically: 3d surface rendering, 3d multiplanar reconstruction, color doppler 3d multiplanar reco.
  • Action
    Siemens issued an Urgent Medical Device Notification to consignees 9/18/07, under Siemens update program US014/07/S. (Distribution on this product had ceased on 6/29/2005.) The firm has instructed the user to not take measurements or use measurements on these secondary captures under the conditions described in the notice, to place a copy of the instructions for use in the file, and to notify all users of the issue with the software. The Siemens Service organization has coordinated the implementation of the field correction with the distributors for all countries. Non-responding consignees will be visited or called by telephone for follow up.

Device

ACUSON Aspen Diagnostic Ultrasound System
  • Modèle / numéro de série
    Serial Numbers: 32118 30032 33270 31789 30264 32770 33492 34115 22353203 40039-1 33468 33732 33808 33867 33906 33972 34080 34085 34104 34161 34168 34174 40009 40024 40046 40062 40093 40094 40101 40102 40132 40148 40163 40178 40187 40189 40197 40257 32603 33548 32611 30509 30991 31397 31770 31824 32018 32090 32551 32738 32927 31214 31518 30803 30828 31805 31875 33209 32053 32319 32497 32531 32830 33505 33421 32140 33515 33347 31997 30640 32141 32208 32209 32251 32450 32582 32625 32646 32796 32819 32886 32965 33020 33197 33206 33239 33269 33338 33454 33470 33494 32321 32117 32784 32831 32926 32581 31218 32992 33514 31117 33358 32674 31975 32539 32686 33712 31995 32718 31270 31804 33650 33433 32700 30167 33227 33757 33910 33796 33390 33098 33781 33995 33882 33516 33974 33709 33973 33992 31124 31619 33193 30033 31520 31876 30555 31335 30176 30472 33742 32741 32884 32887 30382 31599 32701 33432 32934 32761 32932 32540 32762 32827 32736 33041 32554 32583 33024 32978 32365 32496 32338 32449 32473 32917 32918 32514 32510 32222 32856 33059 32891 32877 33044 33049 33276 30412 30575 33300 31471 30993 31131 31363 33416 33261 33244 33230 33131 31810 31856 32042 33431 33195 33089 33162 33285 33060 33196 33101 33544 33070 31746 33283 33229 32143 33452 33517 33105 31367 33310 33724 33403 30834 33559 33587 33624 33652 30715 30315 33797 33774 33399 32772 32168 33032 31055 30695 33561 33672 32955 31976 31241 Material Number 8247888-- with Serial Numbers: 31116 32673 32783 33143 31359 31775 32848 32968 Material Number 8253683: with Serial Numbers: 40290 40311
  • Classification du dispositif
    Radiology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution --- including USA and countries of Argentina, Australia, Austria, Belgium, Brazil, China, Czech Republic, Denmark, Egypt, France, Germany, Great Britain (UK), Greece, Hong Kong, India, Italy, Jordan, Malaysia, Norway, Poland, Portugal, Romania, Russian Federation, Sweden, Switzerland, Thailand, and Turkey.
  • Description du dispositif
    Siemans- ACUSON Aspen Diagnostic Ultrasound System, general purpose Diagnostic Ultrasound system, Model Number: 8247887, Siemans, Mountain View, CA 94039
  • Manufacturer
    Siemens Medical Solutions USA, Inc.

Manufacturer

Siemens Medical Solutions USA, Inc.
  • Adresse du fabricant
    Siemens Medical Solutions USA, Inc., 1230 Shorebire Way, P.O. Box 7393, Mountain View CA 94043
  • Société-mère du fabricant (2017)
    Siemens Ag
  • Source
    USFDA