VITROS Immunodiagnostic Products Signal Reagent. An in vitro diagnostic medical device (IVD) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Ortho-Clinical Diagnostics 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-2017-RN-01090-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2017-08-29
  • 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
    Ortho clinical diagnostics (ocd) updated the reagent pack (i.E. bottle) for vitros signal reagent, beginning with lot 4492. some customers have reported that their vitros 3600 or 5600 system cannot detect the presence of the vitros signal reagent pack when using lot 4492 or above.An investigation by ocd determined that sensors on the vitros system may not detect the base of the updated vitros signal reagent packs due to a larger indentation at the base of the reagent pack. as a result, some vitros 3600 or 5600 systems may not be able to continually detect vitros signal reagent packs in the load positions or during testing at the in-use position.If the sensor cannot detect the base of the pack, that pack cannot be used to process samples.
  • 조치
    If the VITROS 3600 or 5600 System cannot detect the presence of VITROS Signal Reagent Packs, users are to contact the Ortho Care Technical Solutions Centre for immediate assistance. An Ortho trained service representative will schedule the installation of MOD C3. Complete the Confirmation of Receipt form supplied with customer letter and if the affected lots were distributed to a different location, please forward the notification on.

Device

  • 모델명 / 제조번호(시리얼번호)
    VITROS Immunodiagnostic Products Signal Reagent. An in vitro diagnostic medical device (IVD)Product Code: 1072693Lot Numbers: 4492 and aboveExpiry: 13 Aug 2017 and later (as until this issue is resolved, future lots may be affected)ARTG: 180199
  • Manufacturer

Manufacturer