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EXTENSION SET Adverse Event — Malfunction (MDR 9616066-2020-01377)

EXTENSION SET Adverse Event — Malfunction (MDR 9616066-2020-01377) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: EXTENSION SET; Generic name: SET,ADMINISTRATION,INTRAVASCULAR; Manufacturer: CAREFUSION.

DeviceEXTENSION SET
Generic nameSET,ADMINISTRATION,INTRAVASCULAR
ManufacturerCAREFUSION
Report number9616066-2020-01377
Event typeMalfunction
Product problemY
Date received2020-04-28
Report sourceFOREIGN, OTHER
NarrativeALTHOUGH REQUESTED, DEVICE HAS NOT BEEN RECEIVED. A FOLLOW UP REPORT WILL BE SUBMITTED WITH FAILURE INVESTIGATION RESULTS SHOULD THE DEVICE BE RECEIVED FOR EVALUATION.
SourceopenFDA MAUDE (device adverse events)

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