Device Recall FLEXICAIR MC3 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Hill-Rom Manufacturing, Inc. 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
    27202
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-0059-04
  • 사례 시작날짜
    2003-08-27
  • 사례 출판 날짜
    2003-10-24
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2004-07-01
  • 사례 출처
    USFDA
  • 사례 출처 URL
  • 비고 / 경고
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • 데이터 추가 비고
    Bed, Flotation Therapy, Powered - Product Code IOQ
  • 원인
    Reports of patient entrapment between mattress and side-rails.
  • 조치
    Consignees were notified by letter on 08/27/2003. They were alerted to the potential for patient entrapment. Modification of the units were to be conducted at the rental service center, or the sight where the unit is currently located. The consignee would be contacted to arrange for the modification to be installed on the rental if it is at their location when the modification is scheduled for the unit. If the consignee purchased the bed, they would be contacted by a Hill Rom service representative to arrange to install the modification.Enclosed with the letter is information regarding, Tips For Reducing the Risk of Patient Entrapment.

Device

  • 모델명 / 제조번호(시리얼번호)
    MC3, Serial numbers: IC xxxxxx (where xxxxxxx is a 6-digit number sequence).
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Product is distributed through rental and sale nationwide, Canada, Austria, Germany and the U.K.
  • 제품 설명
    FLEXICAIR MC3¿ Low Airloss Therapy unit
  • Manufacturer

Manufacturer

  • 제조사 주소
    Hill-Rom Manufacturing, Inc., 4349 Corporate Road, Charleston SC 29405
  • Source
    USFDA