Retractor for Sciatic Nerve; and Retractor for Sciatic Nerve, long 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes 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-2015-RN-00938-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2015-09-18
  • 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
    Johnson & johnson medical pty. ltd. (jjm) is issuing a medical device recall of certain lots of the depuy synthes sciatic nerve retractors, which are found in the 3.5mm low profile pelvic system. please note that there is no replacement for these products available at this time. micropores may form on the hollow handle of the sciatic nerve retractor during the manufacturing process that are large enough to allow fluids to enter and exit the hollow handle.Even with diligent reprocessing/sterilization of the retractor, subsequent patient(s) may be at risk for infection and adverse tissue reaction due to retained fluids leaking out during use. in the event that the liquid and/or discoloration is not identified preoperatively and enters the operative theatre, there is the potential for surgical delay while a replacement or alternate retractor is requesteda surgical delay may also occur.
  • 조치
    Customers are asked to inspect stock on hand and to quarantine affected units prior to return to JJM for a replacement or an account credit. This action has been closed-out on 05/09/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    Retractor for Sciatic Nerve; and Retractor for Sciatic Nerve, longPart No’s: 03.100.013 and 03.100.014 Multiple lot numbers affectedARTG Number: 155807
  • Manufacturer

Manufacturer