I can just speak to the special access program if we're talking about gel-filled implants. If a gel-filled implant is accessed through the special access program, there's a requirement to report any adverse event associated with it to Health Canada within 72 hours. So there is a requirement to get that information on the device.
In terms of how it's dealt with at the practitional level for removal, that's actually a practice of medicine issue, so I would probably direct that to Dr. Brown.