Events

Device Recall IntraAortic Balloon Catheter Mega 7.5FR 40cc 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Datascope Corporation 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
    79646
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-1383-2018
  • 사례 시작날짜
    2018-02-21
  • 사례 출판 날짜
    2018-04-16
  • 사례 상황
    Open, Classified
  • 사례 국가
    United States
  • 사례 출처
    USFDA
  • 사례 출처 URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=162890
  • 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
    System, balloon, intra-aortic and control - Product Code DSP
  • 원인
    The u.S. instructions for use for the mega intra-aortic balloon (iab) catheter was missing the contraindications section.
  • 조치
    Maquet/Getinge issued a recall letter on February 21, 2018 to affected customers, via FEDEX with confirmation of delivery, to notify them of the fact that the IFU is missing the Contraindications section and to provide the missing information. Affected customers are instructed to examine their inventory immediately to determine if they have affected product. An Addendum to the Mega IAB Catheter IFU, containing the Contraindications, is provided as an attachment in the recall letter. It is suggested that affected customers post copies of the Addendum near all affected lot numbers of Mega IAB Catheters. Customers are provided with Maquet/Getinge contact information should their facility require a full copy of the correct Mega IAB Catheter IFU. Lastly, affected customers are instructed to complete and sign a response form, acknowledging that they have received the notification, and return the form to Maquet/Getinge.

Device

Device Recall IntraAortic Balloon Catheter Mega 7.5FR 40cc
  • 모델명 / 제조번호(시리얼번호)
    0684 00 0295 01U and 0684 00 0295 02U
  • 의료기기 분류등급
    Cardiovascular Devices
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    US Nationwide Distribution
  • 제품 설명
    Intra-Aortic Balloon Catheter Mega 7.5FR 40cc || Product Usage: || The intra-aortic balloon catheter and accessories are used to provide counter pulsation therapy in the aorta, whereby balloon inflation during diastole and deflation during systole increases blood supply to the heart muscle and decreases the work of the left ventricle.
  • Manufacturer
    Datascope Corporation

Manufacturer

Datascope Corporation
  • 제조사 주소
    Datascope Corporation, 15 Law Dr, Fairfield NJ 07004-3206
  • 제조사 모회사 (2017)
    Getinge AB
  • Source
    USFDA