Cook Multi-Use Holmium Laser Fibers 에 대한 현장 안전성 서한
Agency for Medicinal Products and Medical Devices of the Republic of Slovenia (via FOI)에 따르면, 해당 현장 안전성 서한 는
Slovenia
에서 Cook Medical Europe 에 의해 제조된 제품과 관련되어 있습니다.
이것은 무엇인가요?
현장 안전성 서한은 의료기기 제조사 또는 제조사 대리인이 시중에 유통되고 있는 자사 의료기기 제품에 대하여 취할 수 있는 조치를 알리는 소통방식입니다. 주요 대상층은 보건의료업계 종사자와 의료기기 사용자들입니다. 여기에는 회수(recall) 조치와 경고도 포함될 수 있습니다.
Data from Slovenia is current through February 2019. All of the data comes from the Agency for Medicinal Products and Medical Devices of the Republic of Slovenia (via FOI), 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 Slovenia.
데이터 추가 비고
원인
Cook medical is initiating a voluntary correction of the products listed above. we have identified that the
reprocessing instructions do not provide sufficiently detailed information for the cleaning, disinfection, and
sterilization of these products. our preliminary investigation indicates that validation data related to the
reprocessing of these devices do not meet the current guidance.
there have been no reports of adverse reactions related to inadequate cleaning, disinfection, or
sterilization associated with these devices.
potential adverse events that may occur if the products are not adequately reprocessed include
urological infections and systemic infections from a urological origin as well as events resulting from
chemical residual exposure. .