wbd
Electrical
- May 17, 2001
- 658
I am wondering what responsibility I have to notify regulators of an adverse condition at a medical facility. The situation is that about 8 yrs ago I did an electrical study of a hospital that included short circuit,protection,coordination and arc flash, The hospital has 4 emergency generators connected to an emergency bus with 7 breakers that go to the ATS's. During the coordination, I found that 4 emergency generator breakers were set lower than the 7 feeder breakers such that a fault on any one of the feeder circuits would trip off all emergency generators before the specific faulted feeder breaker tripped. This would lead to a complete loss of power in the facility.
I updated the report last year due to some new construction and incorporated the new utility fault currents. I also requested verification of any of the recommended changes from the previous report including the emergency generator breaker setpoint changes. I was told that no changes were made.
Since this is obviously not a desirable condition and does not meet code, what obligation am I under to report this to the regulators if the hospital does not seem to want to make any changes?
Obviously, I am a PE in the state where this study was done.
I updated the report last year due to some new construction and incorporated the new utility fault currents. I also requested verification of any of the recommended changes from the previous report including the emergency generator breaker setpoint changes. I was told that no changes were made.
Since this is obviously not a desirable condition and does not meet code, what obligation am I under to report this to the regulators if the hospital does not seem to want to make any changes?
Obviously, I am a PE in the state where this study was done.