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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...
| Autores principales: | , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
JMIR Publications
2019
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| Materias: | |
| 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 |