Welch Allyn Vital Signs Monitor 5300 Series 300 || Part numbers 007-0098-00 through 007-0159-00 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Welch Allyn Protocol, 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
    29233
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-1333-04
  • 사례 시작날짜
    2004-06-08
  • 사례 출판 날짜
    2004-08-10
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2006-06-21
  • 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
    Oximeter - Product Code DQA
  • 원인
    Potential speaker failure could result in absence of audible annunciation of pulse tones, patient alarms and equipment alerts.
  • 조치
    The firm contacted their customers and their distributors customers via letters dated June 8, 2004 through July 9, 2004. The letters instruct their customers to verify speaker functionality. If the customers do not hear two quick beeps or there is static then they have a faulty speaker. The letters instruct them to stop using the monitor and contact Welch Allyn to have the monitor repaired. If the monitor continues to emit two quick beeps their customers are to contact Welch Allyn to have the monitor repaired as soon as it is convenient. The customers are to verify the two beeps prior to each use. The letter dated June 8, 2004 went to only a couple of direct customers. The remaining letters dated June 14, 2004, June 23, 2004, June 30, 2004 and July 9, 2004 went to direct customers, distributors and distributors'' end user customers.

Device

  • 모델명 / 제조번호(시리얼번호)
    Serial numbers JA000225 through JA002052.
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Welch Allyn distributes product to hospitals, physicians and distributors nationwide and internationally.
  • 제품 설명
    Welch Allyn Vital Signs Monitor 5300 Series 300 || Part numbers 007-0098-00 through 007-0159-00
  • Manufacturer

Manufacturer

  • 제조사 주소
    Welch Allyn Protocol, Inc, 8500 SW Creekside Pl, Beaverton OR 97008-7107
  • Source
    USFDA