BVM (Bag-Valve-Mask) Manual Resuscitation Systems 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 Intersurgical Ltd 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
There is a possibility the valve of the bvm manual
resuscitation system may become stuck during storage. this could result in the
intended tidal volume not being delivered through the valve, which may cause a delay in
treatment.
the instructions for use provided with these products include the requirement to ensure
the bag, valve and oxygen delivery is functioning correctly prior to use. this field safety
notice gives additional information relating to this specific problem and the additional
actions required. .
1. All lot numbers up to and including lot 370253
2. All lot numbers up to and including lot 1170673
3. All lot numbers up to and including lot 31753734
4. All lot numbers up to and including lot 170504