SofPort Advanced Optics Aspheric IOL 의 리콜

Department of Health, Therapeutic Goods Administration에 따르면, 해당 리콜 는 Australia 에서 Bausch & Lomb Australia Pty Ltd 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
    RC-2015-RN-00477-1
  • 사례 위험등급
    Class II
  • 사례 시작날짜
    2015-06-05
  • 사례 국가
  • 사례 출처
    DHTGA
  • 사례 출처 URL
  • 비고 / 경고
    Australian data is current through July 2018. All of the data comes from the Australian Therapeutic Goods Administration, 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 Australia.
  • 데이터 추가 비고
  • 원인
    An investigation was initiated based on a limited number of complaints received for broken haptics during lens loading and insertion. this investigation resulted in bausch + lomb determining that a portion of a batch of haptic material is performing differently than other batches in terms of material elongation properties. a broken haptic during lens loading and insertion can result in surgical intervention (lens exchange) and increase the chance of damaging the eye. there have not been any reports of the haptic breaking after the surgery is complete.
  • 조치
    Customers are advised to segregate the affected IOLs and return them to their Bausch + Lomb (Australia) (B&L;) representative. The B&L; representative will arrange for the provision of replacement stock. If replacement product is needed for a scheduled surgery before the full return can be processed, please contact the B&L; representative to expedite shipment of the IOL. Surgeons are advised that if they have already implanted an affected IOL, there is no indication that the implanted IOL presents a health issue or performance concern. Therefore, patients should be followed as per their usual standard of care. All reports of broken haptics have occurred during lens loading or insertion. This could result in the need to exchange the lens during surgery. This action has been closed-out on 11/08/2016.

Device

  • 모델명 / 제조번호(시리얼번호)
    SofPort Advanced Optics Aspheric IOL, Model LI61AOLI61AO 13.00MM 22.5Serial No.:4464602066Expiry Date: 31-Aug-19LI61AO 13.00MM 23.50Serial No.: 4464642033Expiry Date: 31-Aug-19ARTG No: 98915
  • Manufacturer

Manufacturer