A Hazard Analysis of Class I Recalls of Infusion Pumps

BACKGROUND: The adverse event report of medical devices is one of the postmarket surveillance tools used by regulators to monitor device performance, detect potential device-related safety issues, and contribute to benefit-risk assessments of these products. However, with the development of the rela...

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Detalles Bibliográficos
Autores principales: Gao, Xuemei, Wen, Qiang, Duan, Xiaolian, Jin, Wei, Tang, Xiaohong, Zhong, Ling, Xia, Shitao, Feng, Hailing, Zhong, Daidi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: JMIR Publications 2019
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6524450/
https://www.ncbi.nlm.nih.gov/pubmed/31066695
http://dx.doi.org/10.2196/10366

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6524450/
https://www.ncbi.nlm.nih.gov/pubmed/31066695
http://dx.doi.org/10.2196/10366

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