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PCA Adverse Event — Malfunction (MDR MW1011543)

PCA Adverse Event — Malfunction (MDR MW1011543) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PCA; Generic name: INFUSION PUMP - PATIENT CONTROLLED; Manufacturer: BAXTER HEALTHCARE CORP. ELECTRONIC INFUSION SYS..

DevicePCA
Generic nameINFUSION PUMP - PATIENT CONTROLLED
ManufacturerBAXTER HEALTHCARE CORP. ELECTRONIC INFUSION SYS.
Report numberMW1011543
Event typeMalfunction
Product problemY
Date received1997-06-24
NarrativePT WAS PUT ON MORPHINE TO BE ADMINISTERED BY PCA INFUSION PUMP. PUMP VALUES INDICATED THAT THE MEDICATION WAS DISPENSED. EIGHT HOURS LATER IT WAS DISCOVERED THAT THE PLUNGER HAD MALFUNCTIONED, AND THAT THE SYRINGE WAS FULL AND NO MORPHINE WAS ADMINISTERED.
SourceopenFDA MAUDE (device adverse events)

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