VANGUARD TOTAL KNEE SYSTEM - DCM - PS PLUS TIBIAL BEARINGS 의 리콜

Health Canada (via FOI)에 따르면, 해당 리콜 는 Canada 에서 ZIMMER BIOMET CANADA 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
    120077
  • 사례 위험등급
    I
  • 사례 시작날짜
    2017-02-21
  • 사례 국가
  • 사례 출처
    HC
  • 비고 / 경고
    Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
  • 데이터 추가 비고
  • 원인
    Zimmer biomet is conducting a lot specific medical device field action for various polyethylene implants. the affected products are being removed due to the potential presence of elevated endotoxin levels that exceed the specification limit. the issue was discovered during routine bacterial endotoxin testing (bet). there have been no complaints received related to this issue. endotoxins (pyrogens) are substances found in certain bacteria. the fda-adopted standard for endotoxin levels is 20 eu/device. there were three samples during an approximate 6 week period that were found to exceed this level. as a result the devices manufactured during this period are being removed.

Device

  • 모델명 / 제조번호(시리얼번호)
    Model Catalog: 183740 (Lot serial: >100 LOT NUMBERS CONTACT MFR); Model Catalog: XL-105925 (Lot serial: >100 LOT NUMBERS CONTACT MFR); Model Catalog: XL-105924 (Lot serial: >100 LOT NUMBERS CONTACT MFR); Model Catalog: XL-105923 (Lot serial: >100 LOT NUMBERS CONTACT MFR); Model Catalog: XL-105914 (Lot serial: >100 LOT NUMBERS CONTACT MFR); Model Catalog: XL-105903 (Lot serial: >100 LOT NUMBERS CONTACT MFR); Model Catalog: XL-105833 (Lot serial: >100 LOT NUMBERS CONTACT MFR); Model Catalog: 141514 (Lot serial: >100 LOT NUMBERS CONTACT MFR); Model Catalog: 189080 (Lot serial: >100 LOT NUMBERS CONTACT MFR); Model Catalog: 189062 (Lot serial: >100 LOT NUMBERS CONTACT MFR); Model Catalog: 189040 (Lot serial: >100 LOT NUMBERS CONTACT MFR); Model Catalog: 189020 (Lot serial: >100 LOT NUMBERS CONTACT MFR); Model Catalog: 11-165236 (Lot serial: >100 LOT NUMBERS CONTACT MFR); Model Catalog: 11-165232 (Lot serial: >100 LOT NUMBERS CONTACT MFR); Model Catalog: 11-165226 (Lot serial: >100 LOT NUMBERS CONTACT MFR); Model
  • 의료기기 분류등급
  • 제품 설명
    VANGUARD TOTAL KNEE SYSTEM - DCM - PS PLUS TIBIAL;ARCOMXL RINGLOC LINER;MAXIM KNEE SYSTEM-STEMMED TIBIAL TRAY COMPONENT;TOTAL KNEE SYSTEM - ANTERIOR STABILIZED BEARINGS;RINGLOC BIPOLAR ACETABULAR COMPONENT;MAXIM KNEE SYSTEM-PRIMARY TIBIAL TRAY;HYBRID GLEN
  • Manufacturer

Manufacturer

  • 제조사 주소
    MISSISSAUGA
  • 제조사 모회사 (2017)
  • 제조사 의견
    “The safety of patients has always been, and continues to be, Zimmer Biomet’s top priority and it is our honor to be a leader in this industry for the past 90 years,” Zimmer Biomet told ICIJ in a statement. “We adhere to strict regulatory standards, and work closely with the FDA and all applicable regulatory agencies in each of our regions as part of our commitment to operating a first-rate quality management system across our global manufacturing network. The company added that it is focused on staying at the forefront of innovation and doing right by the millions of patients who rely on the company’s products.
  • Source
    HC