A customer initially reported during the adc device insertion, the sensor did not apply to the skin.A replacement device was ordered however, due to a delivery issue, the customer did not receive the replacement order, therefore, was unable to monitor their blood glucose.The customer experienced blur vision and a loss of consciousness and was unable to self-treat.The customer had contact with a healthcare professional who obtained an unspecified laboratory result and provided glucose via iv for the diagnosis of hypoglycemia.There was no report of death or permanent injury associated with this event.
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