Panthera-Puncher 9, An in vitro diagnostic medical device (IVD) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 PerkinElmer 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-2014-RN-00714-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2014-07-03
  • 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
    Wallac oy, a subsidiary of perkinelmer, has become aware that extended exposure to the ioniser pins of the panthera-puncher 9 can decrease the reaction signal level of assays using antibody coated microtiter plates (such as immunoassays). wallac oy's investigation has shown that uncoated plates are not affected by the phenomenon (such as enzymatic assays). the phenomenon has been determined to be localised to those wells that are located beneath or adjacent to the ioniser pins when the panthera-puncher 9 is idle or in sleep mode. the software allows the ioniser to remain active when the puncher is idle or has gone into sleep mode. the impact on health is dependant on the assay and the associated disorder the assay screens for in the dried blood spot sample.
  • 조치
    PerkinElmer is advising end users to remove plates from the Panthera-Puncher 9 when not actively punching and processing samples. If plates must reside in the device the plate track hatch should be opened to disrupt power to the ioniser. A PerkinElmer Representative will contact customers to arrange for inspection. Additionally, a software update is under development that will automatically switch off the ioniser when the device is in idle. This action has been closed on 29/01/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    Panthera-Puncher 9, An in vitro diagnostic medical device (IVD)Catalogue Number: 2081-0010Serial Numbers: 20810043, 20810139 and 20810145ARTG Number: 186748
  • Manufacturer

Manufacturer