AIRWAY PRESSURE MONITOR WITH ALARM 302220 OEM MONAHAN 332259

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1994-12-09 for AIRWAY PRESSURE MONITOR WITH ALARM 302220 OEM MONAHAN 332259 manufactured by Respironics.

Event Text Entries

[13401] Mother returned my call (i had been unable to reach family for many days) on 10/18/94 and told me that the pt had died last night (10/17/94) in the hospital. She said she couldn't tell me what had happen but that it started at home and when they got to the hospital the t was clinically brain dead. She said theere was going to be an investigation & wanted our equipment left at home. She also said it was not our fault or the equipment's fault & not to worry.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number36222-1994-09001
MDR Report Key23464
Date Received1994-12-09
Date of Report1994-10-26
Date of Event1994-10-17
Date Facility Aware1994-10-18
Report Date1994-10-26
Date Reported to FDA1994-10-26
Date Reported to Mfgr1994-10-26
Date Added to Maude1995-07-14
Event Key0
Report Source CodeDistributor report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameAIRWAY PRESSURE MONITOR WITH ALARM
Generic NameAIRWAY PRESSURE MONITOR
Product CodeCAP
Date Received1994-12-09
Model Number302220 OEM MONAHAN
Catalog Number332259
Lot NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeNO INFO
Implant FlagN
Date RemovedB
Device Sequence No1
Device Event Key23747
ManufacturerRESPIRONICS
Manufacturer Address1001 MURRAY RIDGE DRIVE MURRYSVILLE 3 PA 156688550 US


Patients

Patient NumberTreatmentOutcomeDate
101. Death 1994-12-09

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