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A Hazard Analysis of Class I Recalls of Infusion Pump (Preprint)
2018
JMIR Human Factors
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 related technologies and market, the number of adverse events has also been on the rise, which in turn results in the need to develop efficient tools that help to analyze adverse events monitoring data and to
doi:10.2196/10366
pmid:31066695
pmcid:PMC6524450
fatcat:uewivk7bofatvmvi4a223gbope