Events

PainPump2 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
    56695
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-2592-2010
  • 사례 시작날짜
    2010-09-02
  • 사례 출판 날짜
    2010-09-28
  • 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=94301
  • 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
    Infusion Pump - Product Code FRN
  • 원인
    All of the failures lead to the patient receiving less medication than intended. certain lots of the pain pump have a high failure rate associated with a cracked port housing which leads to internal or external leaks. some lots have a high failure rate associated with e2 errors.
  • 조치
    The firm sent our Urgent Medical Device Recall Notices dated 7/12/2010 to Risk Managers and Materials Managers. The recall notice listed specific lots of PainPump2 and PainPump2 BlockAid that were under recall. Consignees were told to check stock for the recalled product, quarantine the product, and contact Stryker to arrange return shipment of the recalled product. On 9/2/2010 the firm sent out a second Urgent Medical Device Recall Notice. This notice expanded the scope of the recall to include all products distributed within the past 12 months. The shelf life of the product is 1 year -so the recall was for all product currently in the supply chain. The letter again directed consignees to locate the recalled products and contact Stryker to arrange return shipment of the recalled product. The firm sent an additional letter dated 9/1/2010 to its customers. This letter stated that Stryker will no longer be offering any of their PainPump2 products.

Device

PainPump2
  • 모델명 / 제조번호(시리얼번호)
    09232012, '10112032, '09238012, '10113012, '09246012, '10116022, '09259012, '10117012, '09266012, '10118012, '09280012, '10119012, '09287012, '10120012, '09300012, '10123022, '09303012, '10124012, '10005012, '10153012, '10007012, '10154012, '10008012, '10155012, '10011012, '10158022, '10047012, '10159012, '10048012, '10160012, '10049012, '10161012, '10050012, '10162012, '10074022, '10165022, '10076012, '10166012, '10077012, '10167012, '10078012, '10167022, '10081022, '10168012, '10102022, '10169012, '10103012, '10170012, '10104012, '10172022, '10105012, '10173012, '10106012, '10174012, '10109022, '10175012, '10110012, '10176012, '10111022, and '10177012.
  • 의료기기 분류등급
    General Hospital and Personal Use Devices
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Worldwide Distribution -- US, Canada, and Australia.
  • 제품 설명
    Stryker PainPump2 400 mL PainPump with Luer Lock Tubing Set, sterile, REF 540-350, Stryker Instruments, Kalamazoo, MI. || Delivers controlled amounts of medication and narcotics.
  • 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