Oscillating Saw Attachment for Colibri/Colibri II Small Electric Drive (Battery-driven, cutting power tool system used in surgical procedures such as cutting of bone and hard tissue) 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-00353-1
  • 사례 위험등급
    Class I
  • 사례 시작날짜
    2015-04-23
  • 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
    Johnson & johnson medical pty limited (jjm) has received reports that the oscillating saw attachment may disengage intra-operatively. if the device is tested in the operative theatre and the unit does not function, the user most likely would discontinue use of the affected part, and a replacement oscillating saw attachment would be procured, which may lead to surgical delay. injury to the patient can occur if the attachment disengages intra-operatively. there is also a potential of injury to the user from the sharp edge of the subject oscillating saw during retrieval. one report of a serious injury was received where the part fell apart during surgery and resulted in cuts in the hand of a user.
  • 조치
    Johnson & Johnson Medical Pty Limited (JJM) is providing instructions to customers for checking for any disassembly of the attachment as part of every reprocessing cycle. If customers notice any disassembly of the attachment or are able to unscrew the attachment as part of the inspection, they are advised to not use it and immediately send it for repair. Devices which perform satisfactorily during the inspection may be used as intended. A review and repair will be implemented if necessary during the next scheduled maintenance inspection at the Service Centre. Customers are also reminded to ensure the devices are sent for maintenance according to the recommended annual schedule.

Device

  • 모델명 / 제조번호(시리얼번호)
    Oscillating Saw Attachment for Colibri/Colibri II Small Electric Drive (Battery-driven, cutting power tool system used in surgical procedures such as cutting of bone and hard tissue)Part Number (Saw Attachment): 532.021All Serial NumbersProduct Numbers (Electric Drive): 532.001, 532.010, 532.101, 532.110 and 05.001.175ARTG number: 157072
  • Manufacturer

Manufacturer