Biosense Webster's Reprocessed SOUNDSTAR eco Diagnostic Ultrasound Catheters 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 STERILMED, 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
    69337
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-0059-2015
  • 사례 출판 날짜
    2014-10-09
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2015-08-11
  • 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
    Reprocessed intravascular ultrasound catheter - Product Code OWQ
  • 원인
    Sterilmed, a division of johnson & johnson medical nv/sa (sterilmed), has become aware of an issue affecting certain lots of reprocessed soundstar® eco diagnostic ultrasound catheters for which sterilmed is the reprocessor and biosense webster is the distributor. sterilmed determined that the units of these lots were incorrectly processed and as a result when the affected catheter is conne.
  • 조치
    Sterilmed sent an "Field Notification" letter dated September 22, 2014, to all affected customers. The letter identified the product the problem and the action needed to be taken by the customer. Actions requested on your part: 1. Read the Description of the Problem section below carefully. 2.Immediately identify and set aside all units from the affected lots of product listed above in a manner that ensures the affected product will not be used. 3. Maintain a copy of this letter with the affected product. 4. Review, complete, sign and return the attached Field Removal Certification Form in accordance with the instructions listed on the form. 5. Arrange for return of any impacted units from the provided list of affected Reprocessed SOUNDSTAR¿ eco Diagnostic Ultrasound Catheters that you may have in your inventory per the instructions on the Field Removal Certification Form. 6. Pass on this notice to anyone in your facility that needs to be informed. 7. If any of the affected Reprocessed SOUNDSTAR¿ eco Diagnostic Ultrasound Catheters have been forwarded to another facility, contact that facility and arrange for the return. 8. Maintain awareness of this notice until all affected product with lot numbers listed above has been returned to Biosense Webster. For questions related to this issue and product return please contact your Biosense Webster sales representative. For further questions please call (763) 488-3400.

Device

  • 모델명 / 제조번호(시리얼번호)
    Lot Numbers: 1717945, 1721574, 1721575 and 1723123  Catalog Nos: M-5723-115, Model Number BIO10438577
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    US Distribution including the states of WA and CA.
  • 제품 설명
    Biosense Webster's Reprocessed SOUNDSTAR¿ eco Diagnostic Ultrasound Catheters, Catalog Nos: M-5723-115, Model Number BIO10438577.
  • Manufacturer

Manufacturer

  • 제조사 주소
    STERILMED, INC., 11400 73rd Ave N, Maple Grove MN 55369-5561
  • 제조사 모회사 (2017)
  • Source
    USFDA