Trade name: OSCILANTE SAW ADAPTER, FOR REF. 532.001 E 532.010 Technical Name: SURGICAL INSTRUMENTS ANVISA Registration Number: 80145901733 Hazard Class: I Affected Model: SYNTHES ROTATIONAL NON-CUTTING INSTRUMENTAL Affected Series Numbers: SKU: 532.021 || Lot: All Serial Numbers 의 안전성 경고

Agência Nacional de Vigilância Sanitária (ANVISA)에 따르면, 해당 안전성 경고 는 Brazil 에서 Johnson & Johnson do Brasil Ind. e Com. de Prod. para Saúde Ltda; Synthes GmbH 에 의해 제조된 제품과 관련되어 있습니다.

이것은 무엇인가요?

안전성 경고는 의료기기 제품과 관련된 중요한 정보와 권고사항을 담고 있습니다. 물론 안전성 경고가 배포되었다고 해서 해당 제품이 무조건 안전하지 않은 제품이라는 것은 아닙니다. 보건의료업계 종사자와 의료기기 사용자들에게 배포되는 안전성 경고에는 회수(recall)도 포함될 수 있습니다. 제조사가 안전성 경고를 작성하기도 하지만, 보건당국에서 작성하는 경우도 있습니다.

데이터에 대해 더 자세히 알아보기 여기
  • 사례 유형
    Safety alert
  • 사례 ID
    2110
  • 날짜
    2016-11-17
  • 사례 국가
  • 사례 출처
    ANVISA
  • 사례 출처 URL
  • 비고 / 경고
    Brazilian data is current through June 2018. All of the data comes from Anvisa, 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 data from the U.S. and Brazil.
  • 데이터 추가 비고
    If you have any of the affected products identified, follow these steps: • Perform inspection as documented in Document 1 (page 5). This inspection step should be part of the entire reprocessing cycle. • If you notice that the connecting piece has disassembled, or if you can not unscrew the part, do not use the product and send it immediately for repair. • Devices that perform satisfactorily during inspection, as described in Document 1, do not need to be returned for repair and may be used as indicated. We will implement a review and repair, if necessary, during your next scheduled maintenance inspection at your designated Synthes Service Center. • Ensure that devices are shipped for maintenance according to the recommended annual schedule. • Ensure that all persons at your facility, who may be involved in this notification, read this letter carefully. • Keep a copy of this notice with the affected product (s) listed above. • Complete the Verification Section (page 4 of this letter), marking the appropriate field to indicate that the affected product was located and inspected. In addition, indicate which inspected serial numbers are acceptable and which must be returned for service. Enter your name, title, address, phone number and signature in the spaces provided. • Return the completed Verification Section to your local DePuy Synthes contact. • To arrange for the technical assistance of the devices, contact your local DePuy Synthes sales organization.
  • 원인
    It has been reported that the oscillating saw connection part may loosen during surgery.
  • 조치
    Field Action Code R2014068 triggered under the responsibility of Johnson & Johnson do Brasil Ind. And Com. De Prod. for Health Ltda. Company will make correction in the field.