This is an absolutely timely topic and I’ve just recently come across pretty relevant news and articles focusing on whether patients should get access to source codes and data provided by their implantable devices. A few examples:
Hugo Campos has a small computer buried in his chest to help keep him alive. But he has no idea what it says about his faulty heart.
All the raw data it collects, especially any erratic rhythms it controls with shocks, goes directly to the manufacturer. And some of it later gets sent to his doctor.
Lawyer Karen Sandler’s heart condition means she needs a pacemaker-defibrillator to avoid sudden death, so she has one simple question: what software does it run?
Yet it turns out that it’s impossible for her to see and understand the technology that’s being installed into her own body and upon which her life depends. Regulatory authorities don’t see or review the software either.
My two cents here? They DO have access to any kind of data related to their health. But what do you think?