AECL Thera-X25

"This is not a whole body radiation dose. This is just to a very small area," he says. "It was initiated and the machine shut down after five seconds reporting a H tilt error" The FDA protocol at the time was that reports regarding medical devices could only be made by the medical device producers and importers, not by end users or patients. 'If the Canadians don't want to do shit about it, something you can do'