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MICROPUNCTURE Adverse Event — Malfunction (MDR 10004589)

MICROPUNCTURE Adverse Event — Malfunction (MDR 10004589) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: MICROPUNCTURE; Generic name: INTRODUCER, CATHETER; Manufacturer: COOK INCORPORATED.

DeviceMICROPUNCTURE
Generic nameINTRODUCER, CATHETER
ManufacturerCOOK INCORPORATED
Report number10004589
Event typeMalfunction
Product problemY
Date received2020-04-28
NarrativeELDERLY FEMALE PATIENT WAS TRANSFERRED FROM ONE ICU TO ANOTHER ICU HAVING BEEN RULED OUT FOR COVID INFECTION. UPON ARRIVAL TO THE NEW ICU THE PATIENT WAS NOTED TO HAVE A MICROPUNCTURE ARTERIAL LINE WHICH WAS IN THE PATIENT'S RIGHT RADIAL ARTERY. THE A-LINE HAD BEEN PLACED THE PREVIOUS DAY. THE ARTERIAL LINE WAS UNABLE TO HAVE BLOOD DRAWN FROM IT AND HAD POOR ARTERIAL WAVEFORM TRACING. THE ARTERIAL
SourceopenFDA MAUDE (device adverse events)

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