Events

Stryker PainPump2 400 mL Painpump with Luer Lock Tubing Set, REF 540-350, Sterile, Rx only, Stryker Instruments, Kalamazoo, MI. 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Stryker Instruments Div. of Stryker 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
    56687
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-0097-2011
  • 사례 시작날짜
    2010-08-16
  • 사례 출판 날짜
    2010-10-20
  • 사례 상황
    Terminated
  • 사례 국가
    United States
  • 사례 종료 날짜
    2011-04-21
  • 사례 출처
    USFDA
  • 사례 출처 URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=94282
  • 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
    Pump, Infusion - Product Code FRN
  • 원인
    The instructions for use (ifu) has been revised for health care professionals. the indication for use has been changed to remove site specific pain management. the firm has revised the warning to not use the pump around joint spaces. a warning has been added regarding the use of the pump with anticoagulants in epidural applications. a special reminder to users to always evaluate the potential.
  • 조치
    Stryker Instruments sent Urgent Medical Device Recall Notification letters dated 8/16/2010 to healthcare professionals. The recall letters outlined the changes for the instructions for the use of these products. The letters informed the healthcare professional to review the new IFU, to distribute the new IFU to all healthcare professionals that use the device, and to complete and return the business reply form. The letters included a complete IFU that was to be used with any remaining stock of devices. Customers should dispose of the old version of the IFU. There is no product being returned for this recall.

Device

Stryker PainPump2 400 mL Painpump with Luer Lock Tubing Set, REF 540-350, Sterile, Rx only, Stry...
  • 모델명 / 제조번호(시리얼번호)
    09162012, '09163012, '09208012, '09215012, '09223012, '09232012, '09238012, '09246012, '09259012, '09266012, '09280012, '09287012, '09300012, '09303012, '09351012, '09352012, '09353012, '09355022, '09356012, '09362022, '10005012, '10007012, '10008012, '10011012, '10047012, '10048012, '10049012, '10050012, '10074022, '10076012, '10077012, '10078012, '10081022, '10102022, '10103012, '10104012, '10105012, '10106012, '10109022, '10110012, '10111022, '10112032, '10113012, '10116022, '10117012, '10118012, '10119012, '10120012, '10123022, '10124012, '10153012, '10154012 and '10155012.
  • 의료기기 분류등급
    General Hospital and Personal Use Devices
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    US, Canada and Australia.
  • 제품 설명
    Stryker PainPump2 400 mL Painpump with Luer Lock Tubing Set, REF 540-350, Sterile, Rx only, Stryker Instruments, Kalamazoo, MI.
  • Manufacturer
    Stryker Instruments Div. of Stryker Corporation

Manufacturer

Stryker Instruments Div. of Stryker Corporation
  • 제조사 주소
    Stryker Instruments Div. of Stryker Corporation, 4100 E. Milham Ave., Kalamazoo MI 49001
  • 제조사 모회사 (2017)
    Stryker
  • Source
    USFDA