CORFLO

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-10-22 for CORFLO manufactured by Avanos Medical, Inc..

MAUDE Entry Details

Report Number9218834
MDR Report Key9218834
Date Received2019-10-22
Date of Report2019-10-02
Date of Event2019-07-21
Report Date2019-10-02
Date Reported to FDA2019-10-02
Date Reported to Mfgr2019-10-22
Date Added to Maude2019-10-22
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationRISK MANAGER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCORFLO
Generic NameTUBE, FEEDING
Product CodeFPD
Date Received2019-10-22
Lot Number0002974341
Device Availability*
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerAVANOS MEDICAL, INC.
Manufacturer Address5405 WINDWARD PARKWAY ALPHARETTA GA 30004 US 30004


Patients

Patient NumberTreatmentOutcomeDate
10 2019-10-22

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