Tag Archives: FDA
Industry stakeholders and consumer advocacy groups have influenced the US government to shift the focus of US healthcare to quality rather than quantity. In order to protect patients and promote public health, legislation has been put in place which ensures that devices are identifiable and secure at all points. This increase in regulation poses some […]
Inadequate instructions, component issues, and assembly errors—those are but some of the causes behind recent medical device recalls and serious warnings announced by the FDA. Here are some of the major medical device failure events since January: 7 Recent Medical Device Failures Catching FDA’s Eye | Qmed.