Figulla Flex II ASD, Figulla Flex II PFO and Occlutech PDA Occluder Cardiac Occluders 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Getz Healthcare 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-2017-RN-00147-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2017-02-03
  • 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
    Occlutech has received a report whereby a customer inadvertently used an expired occlutech flex ii pusher cable and noticed doing so shortly after the implantation procedure. there was no impact on the patient, the procedure or the product performance. occlutech occluders and compatible pusher cables are packaged together into an occlutech product set which also contains the instructions for use and the patient information card. the outer label on the occlutech product set clearly shows the expiration dates of both the occluder and the pusher cable. as these dates can differ from each other, it is important to check both dates to not miss the shortest expiration date.
  • 조치
    Occlutech will in future be implementing a revised Occlutech product set label showing only the shortest expiry date. For current inventory, Getz Healthcare is advising customers to immediately check the expiration dates of the Occlutech Occluder and of the pusher cable as printed on the outer box-label of all products in their current inventory. If one of the expiration dates is exceeded, customers are to block and remove the Occlutech Occluder set containing the expired product from their inventory. Getz will replace all expired stock. End-users are also advised to carefully routinely review the Occutech Occluder set labels prior to use, in accordance the Instructions for Use. This action has been closed-out on 01/03/2018.

Device

  • 모델명 / 제조번호(시리얼번호)
    Figulla Flex II ASD, Figulla Flex II PFO and Occlutech PDA Occluder Cardiac OccludersFigulla Flex II ASDProduct Code: 29ASDxx Figulla Flex II PFOProduct Code: 19PFOxxD Occlutech PDA OccluderProduct Codes: 42PDAxx, 42PDAxxL, 43PDAxxLMultiple Lot NumbersARTG Numbers: 201602, 201603, 219523
  • Manufacturer

Manufacturer