As I mentioned already, the improvement of mandatory reporting of adverse events for all medical devices needs to happen quickly. In particular, it needs to be extended past hospitals and manufacturers to individual practitioners, private clinics and private settings, including long-term care homes and private clinics that have been promised but have not happened yet.
The other aspect of this is the consumer. Up until recently, the way to file an adverse event report for a consumer was very hard to understand and was quite obscure. That's been improved, but there's a long way to go to make that a much more publicly and well-understood system, so we could also get more reporting that way.