Plum A+ Single Channel Family of Infusers 의 안전성 경고

Department of Health에 따르면, 해당 안전성 경고 는 Hong Kong 에서 Hospira 에 의해 제조된 제품과 관련되어 있습니다.

이것은 무엇인가요?

안전성 경고는 의료기기 제품과 관련된 중요한 정보와 권고사항을 담고 있습니다. 물론 안전성 경고가 배포되었다고 해서 해당 제품이 무조건 안전하지 않은 제품이라는 것은 아닙니다. 보건의료업계 종사자와 의료기기 사용자들에게 배포되는 안전성 경고에는 회수(recall)도 포함될 수 있습니다. 제조사가 안전성 경고를 작성하기도 하지만, 보건당국에서 작성하는 경우도 있습니다.

데이터에 대해 더 자세히 알아보기 여기
  • 사례 유형
    Safety alert
  • 날짜
    2012-11-06
  • 사례 출판 날짜
    2012-11-06
  • 사례 국가
  • 사례 출처
    DH
  • 사례 출처 URL
  • 비고 / 경고
    Hong Kong data is current through September 2018. All of the data comes from the Department of Health (Hong Kong), 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 data from the U.S. and Hong Kong.
    ICU Medical, Inc. acquired from Pfizer in early 2017, Hospira Infusion Systems, the portion of Hospira dedicated to develop infusion pumps.
  • 데이터 추가 비고
    Medical Device Safety Alert
  • 원인
    Medical device safety alert: hospira plum a+ single channel family of infusers the medicines and healthcare products regulatory agency (mhra), united kingdom posted a field safety notice concerning plum a+ single channel family of infusers, manufactured by hospira, inc. the affected list numbers were 11005, 11971, 12391 and 20792. hospira issued a field safety notice to inform users that the volume control knob on some plum a+ single channel infusers (located on the back of the infuser) may not function as described in the system operation manual; the direction for” loud” and “quiet” may be reversed. the manual indicates a clockwise rotation of the knob decreases the volume; however, on some of the devices the alarm volume increases when the knob is turned clockwise. in the event the healthcare professional rotates the volume control knob in the direction described in the system operation manual, the audible tone may be the opposite of the desired audio level. while the device will continue to alarm with an audible one of at least 50 dba at the lowest level, inadvertently setting a low tone when a louder level is actually intended may result in an audible alarm that is more difficult to hear. if this happens, it is possible the clinician may not be alerted when an alarm condition occurs and an interruption in therapy may occur. to correct the issue, hospira will update the system operating manual to clarify the instructions for setting the volume. furthermore, hospira will be creating a volume directional label as an additional improvement. for details, please visit the following mhra website: http://www.Mhra.Gov.Uk/safetyinformation/safetywarningsalertsandrecalls/fieldsafetynotices/con199544 if you are in possession of the product, please contact your supplier for necessary actions. posted on 6 november 2012.

Device

  • 모델명 / 제조번호(시리얼번호)
  • 제품 설명
    Medical Device Safety Alert: Hospira Plum A+ Single Channel Family of Infusers
  • Manufacturer

Manufacturer

  • 제조사 모회사 (2017)
  • Source
    DH