Dani
We've had exactly the same problem, which lead to a clinical incident in our trust.
Reported to MHRA and guess what - yep - no action; report logged.
Whilst these are out there, and we have done our duty and reported it to the powers that be, it still feels like an incident waiting to happen. Without spending loads of dosh - which we don't have, I can't see a way out of this without Graseby and MHRA coming forward with a solution.
The problem being of course is that the 3300 is now at or near to the end of its product life and a second modification which will address the design deficiency will probably not be economically viable from the manufacturers point of view.
Might be an interesting debating point in a coroner's court though! Hopefully not one that requires my presence.
Brian
