Device Recall Clinitron Rite Hite Bed headboard and foot side rails. 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 Hill-Rom, 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
    60888
  • 사례 위험등급
    Class 3
  • 사례 연번
    Z-1132-2012
  • 사례 시작날짜
    2012-02-03
  • 사례 출판 날짜
    2012-03-01
  • 사례 상황
    Terminated
  • 사례 국가
  • 사례 종료 날짜
    2012-12-05
  • 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
    Bed, air fluidized - Product Code INX
  • 원인
    The firm identified in october 2011 that the clinitron rite hite bed and clinitron at home bed headboards failed to meet the safety standard force requirements. the firm identified in october 2011 that the clinitron rite hite bed and clinitron at home bed outer rail, which is extruded aluminum tubing, is intended to be one piece joined together by a weld at the lower center. the parts receiv.
  • 조치
    Hill-Rom, Inc. sent a Modification Notice Urgent Medical Device Correction Notification dated February 2, 2012, to all affected customers. The letter identified the product the problem and the action needed to be taken by the customer. The modification notice instructed all customers to find and replace all headboards and food side rails that do not meet design intent. All technicians will inspect all affected product in the service centers and all at home and rite hite beds for an "x" or "L" stamp. The technicians will inspect the beds that are still in use during scheduled maintenance or before each rental. All will be completed before 01-JUL-12. For support call 1-800-445-3720

Device

  • 모델명 / 제조번호(시리얼번호)
    The headboard (p/n 6020200003) and siderail (p/n 6020200002) are not serialized. There are no model, catalog or code number identification marks available on the accessories. It is possible to identify these accessories though by a mark stamped into the mounting post that are used to attach these accessories to the bed. May 2011 and October 2011 headboards and siderails were shipped to customers.
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Worldwide Distribution -- USA (nationwide) including the states of AL, AK, AZ, AR, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, VA, WA, WI, WV, and WY. and the country of Canada.
  • 제품 설명
    Clinitron Rite Hite Bed headboard and foot side rails. || The Clinitron Rite Hite Air Fluidized Therapy Unit is a patient management system that combines air fluidized therapy and low airloss therapy technologies together on a low-height frame. The lower body section provides air fluidized therapy, and the upper body section provides low airloss therapy.
  • Manufacturer

Manufacturer

  • 제조사 주소
    Hill-Rom, Inc., 1069 State Route 46 East, Batesville IN 47006-7520
  • 제조사 모회사 (2017)
  • Source
    USFDA