LIFEGUARD SAFETY INFUSION SET Adverse Event — Malfunction (MDR MW5094270)

Name: LIFEGUARD SAFETY INFUSION SET Adverse Event — Malfunction (MDR MW5094270)
Creator: DeviceEvents

LIFEGUARD SAFETY INFUSION SET Adverse Event — Malfunction (MDR MW5094270) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: LIFEGUARD SAFETY INFUSION SET; Generic name: SET, ADMINISTRATION, INTRAVASCULAR; Manufacturer: VYGON USA.

Device	LIFEGUARD SAFETY INFUSION SET
Generic name	SET, ADMINISTRATION, INTRAVASCULAR
Manufacturer	VYGON USA
Report number	MW5094270
Event type	Malfunction
Product problem	Y
Date received	2020-04-24
Narrative	AN ENTIRE LOT OF HUBER NEEDLES ARE UNABLE TO PRIME/FLUSH. FDA SAFETY REPORT ID# (B)(4).
Source	openFDA MAUDE (device adverse events)

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