OXIMETER, PULSE. PHYSIOLOGICAL MONITORING SYSTEM, NEONATAL. PROBES, OXIMETER. . EQUIPMENT: GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES PHYSIOLOGIC MONITORING SYSTEMS: (1) DASH 2000, (2) DASH 3000, (3) DASH 4000, (4) EAGLE, (5) SOLAR 8000, (6) SOLAR 8000M, 450SL; NELLCOR SPO2 PULSE OXIMETER SENSORS: (8) DISPOSABLE, (9) REUSABLE 의 안전성 경고

Agência Nacional de Vigilância Sanitária (ANVISA)에 따르면, 해당 안전성 경고 는 Brazil 에서 GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES MONITORING DIV [393580], 8200 W TOWER AVE, MILWAUKEE WI 53223-3219; (8 E 9) MALLINCKRODT INC A TYCO HEALTHCARE GROUP CO [225956], PO BOX 5840, ST LOUIS MO 63134 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
  • 사례 ID
    98
  • 날짜
    2001-06-30
  • 사례 국가
  • 사례 출처
    ANVISA
  • 사례 출처 URL
  • 비고 / 경고
    Brazilian data is current through June 2018. All of the data comes from Anvisa, 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 Brazil.
  • 데이터 추가 비고
    UNTIL THIS DATE DOES NOT CONSERT PRODUCT REGISTRATION IN BRAZIL
  • 원인
    A member hospital of the ecri user network expressed the concern that during the monitoring of sp02 in which the ge medical systems information technologies (gems-it) physiological monitoring systems and the above pulse oximetric discharging sensor was used, a disconnection of the patient's sp02 sensor that could not be detected due to the lack of a persistent sound indicator to alert team members. the member hospital declares that, when disposable sensors are used, the monitoring system to which these are connected, indicates the disconnection through a single sound signaling on the side of the bed and on the central monitors, which is less unnelving that the repeating sounds when the sp02 reusable sensors are used. the member hospital declares that, after not being aware of any adverse episode, there is the concern that members of the team can not perceive if the disposable sensors leave the patient. ecri declares that an investigation revealed that this problem occurs with the eagle line monitors or when the multi parameter module or single spo2 parameter modules are used with the solar 8000 monitor. the manufacturer declares that the problem also affects the monitor solar 8000m and the dash monitor line.
  • 조치
    REFER TO THE ORIGINAL REPORT BELOW UNDERSTANDING THE REASON BEHIND THE FOLLOWING RECOMMENDATIONS ECRI RECOMMENDS THE FOLLOWING: (1) NOTIFY THE USERS OF THE GEMS-IT MONITORS OF THE PROBLEM AND THE ECRI REPORT. (2) IF YOUR INSTITUTION USES NELLCOR SP02 DISPOSABLE SENSORS WITH SOLAR 8000M, DASH 3000 OR DASH 4000 MONITORS, GET A NEW GEMS-IT SOFTWARE / PROGRAM WHEN IT IS AVAILABLE (PROGRAM / SOFTWARE VERSIONS AND RELEASE DATES NOT DISCLOSED BY GEMS-IT); THE PROGRAM WILL PRODUCE AN AUDIBLE AND REPEATABLE ALARM FOR PULSE / PULSE SEARCH? (2) NO PROGRAM WILL BE AVAILABLE TO THE EAGLE MONITOR LINE, TO THE DASH 2000 MONITOR OR TO THE OLDEST MONITOR MODELS OF THE SOLAR 8000. (3) IF YOUR USE IS NOT USED OR UNABLE TO USE THE PROGRAM, EMPLOY THE REUTILIZABLE SENSOR UNTIL DISPOSABLE, WHEN POSSIBLE, AND, (3) MAKE SURE TO CONSIDER REGULATORY PATIENT TO MAKE SURE THAT THE SPO2 IS BEING MONITORED CORRECTLY. FOR FURTHER INFORMATION, PLEASE CONTACT RICH DIEFES, ECRI, TELEPHONE (610) 825-6000, RAMAL 5536