Events

Trochar Scalpel Instrument (Surgical Punch) 의 리콜

U.S. Food and Drug Administration에 따르면, 해당 리콜 는 United States 에서 OrthoPediatrics Corp 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
    63396
  • 사례 위험등급
    Class 2
  • 사례 연번
    Z-0207-2013
  • 사례 시작날짜
    2012-09-13
  • 사례 출판 날짜
    2012-11-05
  • 사례 상황
    Terminated
  • 사례 국가
    United States
  • 사례 종료 날짜
    2013-09-18
  • 사례 출처
    USFDA
  • 사례 출처 URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=113679
  • 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
    Mixture, hematology quality control - Product Code HSB
  • 원인
    A complaint received from sales representative that a replenishment instrument was too short. upon investigation, it has been determined that the device was not manufactured to design specifications and will not function as intended.
  • 조치
    OrthoPediatrics Corp sent an Urgent Recall e-mail dated September 14, 2012, to all affected customers. The e-mail identified the product, the problem, and the action to be taken by the customer. Customers were instructed to quarantine all identified devices from the affected lot numbers immediately. Customers were also asked to complete the Mandatory Reply Form. Customers with questions should call 574-268-6379.

Device

Trochar Scalpel Instrument (Surgical Punch)
  • 모델명 / 제조번호(시리얼번호)
    Part number: 01-1500-9014 and Lot #'s 1466707 and 1466710
  • 의료기기 분류등급
    Orthopedic Devices
  • 의료기기 등급
    2
  • 이식된 장치?
    Yes
  • 유통
    Nationwide Distribution including AL, IL, NY, FL, TX, MI, KY, NC, CO, and GA.
  • 제품 설명
    Trochar Scalpel Instrument (Surgical Punch) || OrthoPediatrics intramedullary rods (nails) are generally rod-shaped devices, with screw holes at either end for fixation to bone. This device is intended to be inserted into the medullary canal of the femur for fixation of fractures by aligning and stabilizing the bone fragments. Additional stabilization may be realized by installing transverse screws through holes in the rod. These devices are made of medical grade stainless steel. The OrthoPediatrics PediNail" system is used for pediatric and small stature adult patients as indicated to stabilize fractures of the femoral shaft; subtrochanteric fractures; ipsilateral neck/shaft fractures; prophylactic nailing of impending pathologic fractures; nonunions and malunions; fixation of femurs that have been surgically prepared (osteotomy) for correction of deformity.
  • Manufacturer
    OrthoPediatrics Corp

Manufacturer

OrthoPediatrics Corp
  • 제조사 주소
    OrthoPediatrics Corp, 2850 Frontier Dr, Warsaw IN 46582-7001
  • 제조사 모회사 (2017)
    Orthopediatrics Corp
  • Source
    USFDA