Agency for Medicinal Products and Medical Devices of the Republic of Slovenia (via FOI)에 따르면, 해당 현장 안전성 서한 는
Slovenia
에서 Baxter International, Inc. 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
Baxter healthcare corporation issues a voluntary recall of the hemodialysis conventional product line with the above product codes and batch numbers due to customer complaints regarding fracture of the pre-dialysis artery expansion chamber at various stages of treatment. following an investigation, baxter found that there had been a change in the formulation of the material which could have led to increased material fragility and reduced impact resistance.
114525 BL105 1701 to 1719
between 31.12.2019 and
04/30/2020
114526 BL121P 1701 to 1719
between 31.12.2019 and
04/30/2020
114527 BL130PSN 1701 to 1719
between 31.12.2019 and
04/30/2020
114557 BL208BD 1701 to 1719
between 31.12.2019 and
04/30/2020
114559 BL224BD 1701 to 1719
between 31.12.2019 and
04/30/2020