This text is used as an example, there is no more information provided. The terms I do not understand are "Reference High Panel" and "Reference Low Control". I assume that this is about the manufacturing of medical products where something went wrong. Any help is greatly appreciated (English explanation or German translation suggestion).
Context:
On the 20th July 07, an initial fail was returned for Reference High Panel where an out of specification result of 0.10 uIU/mL was returned for List Number 1L730001, Lot#55910JN00 SO7169. Upon re-test, the Grand Mean Concentration for the Reference Low Control was 0.30 uIU/mL and the Reference High Panel was 0.09 uIU/mL, both out of specification range.