RELIAVAC 400 CLOSED WOUND SUCTION KIT WITH PVC SILICONIZED DRAIN 12.5" Adverse Event — Malfunction (MDR 1018233-2020-02894)

Name: RELIAVAC 400 CLOSED WOUND SUCTION KIT WITH PVC SILICONIZED DRAIN 12.5" Adverse Event — Malfunction (MDR 1018233-2020-02894)
Creator: DeviceEvents

RELIAVAC 400 CLOSED WOUND SUCTION KIT WITH PVC SILICONIZED DRAIN 12.5" Adverse Event — Malfunction (MDR 1018233-2020-02894) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: RELIAVAC 400 CLOSED WOUND SUCTION KIT WITH PVC SILICONIZED DRAIN 12.5"; Generic name: SUCTION EVACUATOR; Ma

Device	RELIAVAC 400 CLOSED WOUND SUCTION KIT WITH PVC SILICONIZED DRAIN 12.5"
Generic name	SUCTION EVACUATOR
Manufacturer	C.R. BARD, INC. (COVINGTON) -1018233
Report number	1018233-2020-02894
Event type	Malfunction
Product problem	Y
Date received	2020-04-28
Report source	DISTRIBUTOR, OTHER
Narrative	IT WAS REPORTED THAT IT WAS DIFFICULT TO INFLATE THE SUCTION EVACUATOR.
Source	openFDA MAUDE (device adverse events)

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