5 Considerations for Minimizing Medical Device Recall Risk
Medical device recall events are on the rise, with reports of recalls increasing by 8.8% from 2021 to 2022. It’s a sobering statistic for those charged with the development and manufacturing of these devices.
In 5 Considerations for Minimizing Medical Device Recall Risk, we examine the most common reasons medical devices are recalled, as well as offer best practices for product design and development teams to help mitigate the risk of such adverse outcomes.
This whitepaper explores:
- What can cause a medical device recall, from component failure to software errors to issues in documentation
- The impacts of medical device recall on both the manufacturer and the general public
- How to mitigate risk during product development with design best practices, component partnerships, testing and more
