Events

Device Recall Model 134, WarmAir Convective Warming Device 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Cincinnati Sub-Zero Products 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
    59018
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-2800-2011
  • 사례 시작날짜
    2011-05-19
  • 사례 출판 날짜
    2011-07-14
  • 사례 상황
    Terminated
  • 사례 국가
    United States
  • 사례 종료 날짜
    2013-02-26
  • 사례 출처
    USFDA
  • 사례 출처 URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=100840
  • 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
    System, thermal regulating - Product Code DWJ
  • 원인
    A component defect. the recalling firm determined that one of the connectors attached to the firm's warmair 134 device's printed circuit board (pcb) can overheat. should this event occur, the excess heat build up within the device may result in damage to the device's external case and/or melting of some of the internal components of the unit.
  • 조치
    CSZ Cincinnati Sub-Zero sent an "URGENT MEDICAL DEVICE RECALL FIELD ACTION" notice to all affected customers. The letter identifies the product, problem, and actions to be taken. CSZ instructs customers to complete and return an enclosed recall response form and to state whether or not their facility is in possession of the device. The completed form should be returned via fax at 513-772-9119 or via e-mail to WA134Recall2011@cszinc.com. Additionally, customers are instructed to discontinue use of the device and return to their Biomedical Engineering and/or Service Department for device exchange and return. Questions regarding this notice are directed to the WarmAir 134 field action (recall) administrator at 1-800-989-7373.

Device

Device Recall Model 134, WarmAir Convective Warming Device
  • 모델명 / 제조번호(시리얼번호)
    Part #86180, Device Listing #D111865, Serial Numbers: 963-1340100 thru 964-1340199; 971-1340200 thru 971-1340294, 973-1340345 thru 973-1340455; 974-1340445 thru 974-1340594; 981-1340605 thru 981-1340674; 983-1340815 thru 983-1340864; 984-1340905 thru 984-1340964; 991-1341025 thru 991-1341064; 992-1341095 thru 992-1341174; 993-1341265 thru 993-1341274; 994-1341365 thru 994-1341374; 001-1341375 thru 001-1341404; 002-1341405 thru 002-1341414; 003-1341415 thru 003-1341424; and 004-1341425-2 thru 004-1341426-2, are subject to recall**.   **Please Note: CSZ serializes the WarmAir 134 devices beginning with the last two digits of the year manufactured, followed by the quarter of manufacture, the numbers "134" and then a sequential number. For example, a unit with serial number 963-1340100 was manufactured in the third quarter of 1996 with a sequential number of 0100.
  • 의료기기 분류등급
    Cardiovascular Devices
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Worldwide Distribution--USA (nationwide) including the states of AL, AR, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, LA, MA, MI, MO, NC, NJ, NM, NV, NY, OH, OK, PA, RI, SC, SD, TN, TX, UT, VA, WA, and WI and the country of Canada.
  • 제품 설명
    Model 134, WarmAir Convective Warming Device, 115V, Part #86180, Device Listing #D111865, The WarmAir 134 is used in conjunction with a single-patient use blanket to warm a patient's body temperature. The device draws in room air through a filter by means of an electric blower. It heats the air to the desired temperature by controlling the air temperature entering a flexible connecting hose, and conveys it to the disposable blanket (i.e. FilteredFlow Blankets, Warming Tube) in contact with the patient, in order to warm the patient. || This device provides a continuous flow of heated air as a means of warming patients suffering the common, but significant problems of hypothermia. The system can be used in Post Anesthesia Care Units (PACUs), Intensive Care Units (ICUs), Surgical Intensive Care Units (SICUs), Emergency Rooms (ERs), Operating Rooms (ORs), or any other departments or hospital facilities requiring patient temperature management.
  • Manufacturer
    Cincinnati Sub-Zero Products Inc

Manufacturer

Cincinnati Sub-Zero Products Inc
  • 제조사 주소
    Cincinnati Sub-Zero Products Inc, 12011 Mosteller Rd, Cincinnati OH 45241
  • 제조사 모회사 (2017)
    Gentherm, Inc.
  • Source
    USFDA