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.
Hong Kong data is current through September 2018. All of the data comes from the Department of Health (Hong Kong), 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 Hong Kong.
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Medical Device Safety Alert
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Field safety notice: smith & nephew 560p high definition camera control unit
medical device manufacturer, smith & nephew inc., issued a field safety notice concerning certain 560p high definition camera control unit [product code: 72201919; serial no.: bbs1203 & bbs1450]. user of the device may experience intermittent loss of video due to a defective board component, which was incorporated during the manufacturing process.
according to the manufacturer, there is a risk of inadvertent damage to non-target tissue while visualization is not functioning correctly if loss of video or display is experienced during the surgical procedure.
according to the local supplier, the affected devices were distributed to hong kong.
for more details, please refer to the attachment. if you are in possession of the product, please contact your supplier for necessary actions.