Cortex Screw Ø 4.5mm, self-tapping, length 20mm, Pure Titanium 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-2016-RN-00570-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2016-05-03
  • 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
    The affected part and lot numbers of the 4.5mm cortex screws, length 20mm, may contain a 4.5mm cortex screw that is 22mm in length; the screws are both etched and labelled with the affected 20mm part numbers.The outside package labelling and the etching on the product would indicate to the user that the screw is 2mm shorter than its actual length of 22mm. if detected prior to insertion it may result in a surgical delay while a replacement is obtained or if the surgeon inserts the screw, determines it was the wrong length on radiographic imaging, and then removes and replaces it.In addition, the potential harm of damage to surrounding structures including damage to articular surface during insertion could occur, depending upon the location and angle of screw. a screw that is too long can also result in soft tissue damage (soft tissue irritation) if not recognised during the procedure. at this time there have been no reports of patient involvement.
  • 조치
    JJM is advising users to inspect stock and quarantine the affected units prior to their return to JJM. Past surgical results should be reviewed at the discretion of the surgeon for patients who have been implanted with screws from this particular lot number. This action has been closed out on 19/01/2017.

Device

Manufacturer