A high reading issue was reported with the adc device.Customer received sensor scan results that were higher when compared to readings obtained on the built-in reader and experienced symptoms described as "sensation of weakness" and loss of balance.Customer was unable to self-treat and required administration of "oral sugaring syrup" by third-party.No additional treatment was reported.There was no report of death or permanent impairment associated with this event.A sensor scan result of 76 mg/dl was compared to a reading of 33 mg/dl obtained on the built-in reader.The results, when plotted, fell into the "c" zone, showing the difference in values to be clinically significant.It is unknown when these readings were obtained in relation to the reported medical event.
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