PHILIPS RESPIRONICS V60 1053616

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-03-23 for PHILIPS RESPIRONICS V60 1053616 manufactured by Respironics California, Inc..

Event Text Entries

[184467191] Patient was found with bipap mask off and machine was shut off and alarming. Machine would not turn back on. Machine continued to alarm when machine off.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9864912
MDR Report Key9864912
Date Received2020-03-23
Date of Report2020-02-12
Date of Event2020-01-17
Report Date2020-02-12
Date Reported to FDA2020-02-12
Date Reported to Mfgr2020-03-23
Date Added to Maude2020-03-23
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag0
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 NamePHILIPS RESPIRONICS
Generic NameVENTILATOR, CONTINUOUS, MINIMAL VENTILATORY SUPPORT,FACILITY USE
Product CodeMNT
Date Received2020-03-23
Model NumberV60
Catalog Number1053616
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerRESPIRONICS CALIFORNIA, INC.
Manufacturer Address2271 COSMOS CT CARLSBAD CA 92011 US 92011


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-23

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