Agency for Medicinal Products and Medical Devices of the Republic of Slovenia (via FOI)에 따르면, 해당 현장 안전성 서한 는
Slovenia
에서 Roche 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
We have become aware of a software issue that may lead to erroneous results on cobas c 111 analyzer (without
ise unit) in very rare cases. cobas c 111 analyzer with ise unit are not affected as long as the ise is in status
‘ready’. to date, no field issue has been reported where the identified software error actually produced wrong
results.
under very rare constellations of already used and unused cuvettes remaining on the cobas c 111 analyzer rotor a
measurement timing error “7002: 108000572 a software error occurred” might be produced. immediately after
occurrence of the error all ongoing tests are stopped. depending on open test orders the system might restart
processing using an already consumed cuvette and hence, producing a potentially erroneous result.
we have identified measures to ensure the detectability for measurements that may have yielded erroneous results.
.