PORT ACCESS NEEDLE Adverse Event — Malfunction (MDR 10000338)

Name: PORT ACCESS NEEDLE Adverse Event — Malfunction (MDR 10000338)
Creator: DeviceEvents

PORT ACCESS NEEDLE Adverse Event — Malfunction (MDR 10000338) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PORT ACCESS NEEDLE; Generic name: SET, ADMINISTRATION, INTRAVASCULAR; Manufacturer: BARD ACCESS SYSTEMS, INC..

Device	PORT ACCESS NEEDLE
Generic name	SET, ADMINISTRATION, INTRAVASCULAR
Manufacturer	BARD ACCESS SYSTEMS, INC.
Report number	10000338
Event type	Malfunction
Product problem	Y
Date received	2020-04-27
Narrative	PORT ACCESS NEEDLE THE LINE BROKE AT WHERE YOU SCREW IN THE CONNECTOR.
Source	openFDA MAUDE (device adverse events)

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