PRIMARY IV CLEARLINK SYSTEM TUBING Adverse Event — Malfunction (MDR 10004551)

Name: PRIMARY IV CLEARLINK SYSTEM TUBING Adverse Event — Malfunction (MDR 10004551)
Creator: DeviceEvents

PRIMARY IV CLEARLINK SYSTEM TUBING Adverse Event — Malfunction (MDR 10004551) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PRIMARY IV CLEARLINK SYSTEM TUBING; Generic name: SET, ADMINISTRATION, INTRAVASCULAR; Manufacturer: BAXTER HEALTHCARE CORPORATION.

Device	PRIMARY IV CLEARLINK SYSTEM TUBING
Generic name	SET, ADMINISTRATION, INTRAVASCULAR
Manufacturer	BAXTER HEALTHCARE CORPORATION
Report number	10004551
Event type	Malfunction
Product problem	Y
Date received	2020-04-28
Narrative	EVENT #1: I WENT INTO THE PATIENTS' ROOM BECAUSE THEIR INFUSION OF VANCOMYCIN WAS COMPLETED. WHEN I ATTEMPTED TO REMOVE THE PRIMARY IV LINE (PAYING ESPECIALLY CLOSE ATTENTION NOT TO STRESS THE END, AND ATTEMPTING TO PULL STRAIGHT OUT) THE END OF THE LINE BROKE OFF INSIDE THE MICROCLAVE. THE CAP WAS IMMEDIATELY REMOVED AND A NEW ONE PRIMED AND USED. THERE WERE NO RESIDUAL BROKEN PIECES IN THE LINE.
Source	openFDA MAUDE (device adverse events)

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