C-series home pump containing fluorouracil / ns mixture dosed at 2400mg/m2/dose (4200mg) iv over 46 hours was started on (b)(6) at 1118 at infusion center with dual rn sign off.Flow restrictor taped to skin, verified clamps are open and verified infusion rate on mar matches c-series pump.On (b)(6) 2022 patient returned to infusion center for scheduled pump disconnect.It was identified that the pump failed to completely deliver its contents.On examination it was estimated that approximately 70% of the contents had infused.A reason for the incomplete discharge of the pump contents could not be determined.All connections intact, there were no kinks in the line, the sensor was still taped to the patients' abdomen, huber needle in place.The patient's port was functioning and had good blood return.The pump was disconnected, and no attempt was made infuse the remainder.Provider notified.
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