VERION Reference Unit (Vision Planner) - used with the Alcon LenSx Laser System (Surgery planning system for ophthalmic surgery) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Alcon Laboratories Australia Pty Ltd 에 의해 제조된 제품과 관련되어 있습니다.

이것은 무엇인가요?

의료기기에 문제가 생겼을 경우 제조사가 이를 바로잡거나 시장에서 회수하는 조치를 말한다. 회수(Recall)는 의료기기에 결함이 있거나, 건강에 위협이 되거나, 또는 결함도 있고 건강에도 위협이 될 경우에 발생한다.

데이터에 대해 더 자세히 알아보기 여기
  • 사례 유형
    Recall
  • 사례 ID
    RC-2016-RN-00255-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2016-03-08
  • 사례 국가
  • 사례 출처
    DHTGA
  • 사례 출처 URL
  • 비고 / 경고
    Australian data is current through July 2018. All of the data comes from the Australian Therapeutic Goods Administration, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Australia.
  • 데이터 추가 비고
  • 원인
    Alcon has received reports concerning the inclusion of unplanned arcuate incisions on printed, saved (.Pdf) or exported surgical plans. this situation only occurs when the verion reference unit (vision planner) is used to create a surgical plan for non-alcon toric intraocular lenses (iols) that is used with the alcon verion digital marker lensx laser system. surgical plans for alcon toric iols as well as all spherical iol regardless of brand are not affected. these unintentional surgical plan arcuates can occur if the deactivated ‘iol 100% – ri 0%’ slider bar is unintentionally activated by the user in the planning software. this directs the software to include the addition of arcuates for the surgical procedure and can only be seen on the exported, saved (.Pdf) or printed surgical plans. if the additional arcuates are performed this may lead to an astigmatism overcorrection resulting in reduced unaided visual acuity.
  • 조치
    Alcon is providing users with work around instructions to follow as an interim measure. A software update will be installed on all affected systems as a permanent fix.

Device

  • 모델명 / 제조번호(시리얼번호)
    VERION Reference Unit (Vision Planner) - used with the Alcon LenSx Laser System (Surgery planning system for ophthalmic surgery)Catalogue Number: 8065998240ARTG Number: 214732
  • Manufacturer

Manufacturer