Resus-EZY Manual Resuscitator (single-use pulmonary resuscitator) 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Schell Medical Corporation 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-2016-RN-00645-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2016-05-12
  • 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
    There have been some reported cases where the flow diverter used in these products is being cracked. the flow diverter is the blue adaptor that attaches to the patient valve. the flow diverter directs the patient’s exhaled breath to atmosphere or into a peep (positive end expiratory pressure)valve where a peep valve is being used. a cracked flow diverter can affect the peep valves ability to hold peep. as the flow diverter is on the expiratory side of the breathing system there is no effect on the resuscitators ability to deliver gas to the patient. additionally, in the event of a cracked flow diverter, there are two discrete one way valves isolating the expiratory side from the inspiratory side. thus there is no pathway by which any foreign material could enter the inspiratory side of the resuscitator. a cracked flow diverter has no affect upon the resuscitators ability to deliver gas to the patient.
  • 조치
    Schell Medical is advising users to inspect stocks for the affected lot numbers. If any of the impacted products show signs of cracking, quarantine for return and replacement by Schell as per normal procedures. This action has been closed-out on 03/02/2017.

Device

  • 모델명 / 제조번호(시리얼번호)
    Resus-EZY Manual Resuscitator (single-use pulmonary resuscitator)Catalogue Numbers: HP-9511E, HP-9511F, HP-9511FL3, HP-9511FN, HP-9511PE, HP-9511PF, HP-9511Z, HP-9611OUENBatch Number: 061115ARTG Number: 93870
  • Manufacturer

Manufacturer