Stratus® CS Acute Care™ Diagnostics System
Stratus® CS 200 Acute Care™ Diagnostics System 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 Siemens Healthcare Diagnostics 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
Siemens healthcare has confirmed a software defect in the stratus cs acute care diagnostics
system and stratus cs 200 acute care diagnostics system regarding testpak calibration and
quality control (qc) status when a testpak is due to expire within 48 hours.
depending on the calibration status, either an above assay range (aar) or an inaccurate
value could potentially be reported when running a testpak that is due to expire within 48
hours.
.
Analyzer Serial Numbers
Stratus® CS 200
Acute Care™
Diagnostics System
10714016 2.0.1 and 2.0.2 All serial numbers
Stratus® CS
Acute Care™
Diagnostics System
10444834
10453531
10453570
10453571
10470384
All software
versions
All serial numbers