BD Vacutainer Multiple Sample Luer Adapter 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Becton Dickinson 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-2013-RN-00335-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2013-04-23
  • 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
    Bd has received a number of following complaints relating to blood leakage when the vacutainer adapter is used in the blood collection process:1)the sleeve covering the np cannula - non-sleeve recovery, sleeve leakage, and sleeve fall off (pop-off). should such an event occur, there is an increased likelihood of blood leakage into the tube holder when a blood collection tube is removed from the tube holder (i.E. the sleeve fails to re-cover the np cannula allowing blood to leak into the tube holder). bd estimates that approximately 1.47% of the devices will be impacted by this issue.2)luer tip damage – small “nicks” or “flash” have been observed on the luer tip that connects to needles, blood collection sets, and infusion sets. should such a damaged device be used, there is an increased likelihood of blood leakage from the connection between the vacutainer adapter r and the access device. bd estimates that less than 1% of the devices will be impacted by this issue.
  • 조치
    BD is requesting customers to consider the risk of using a defective device in relation to their ability to maintain necessary blood collection procedures without the use of the BD Vacutainer Multiple Sample Luer Adapter. Should the customers choose to continue using the BD Vacutainer Multiple Sample Luer Adapter, BD is asking to ensure that all relevant staff are aware of the potential defects. BD also recommends that staff closely observe the luer tip of the device for potential damage. In the event that damage is observed, please instruct staff to discard the individual device. Should blood leak from the luer connection during blood collection please assess the need to conduct a re-draw, with a new luer adaptor, based upon the volume of blood within the tube (i.e. a low volume draw would require a re-draw). This action has been closed-out on 18/02/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    BD Vacutainer Multiple Sample Luer AdapterRef. No.: 367300All lot numbers manufactured starting with lot number 1354918 and afterARTG: 122153
  • Manufacturer

Manufacturer