NELLCOR GR101704

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-02-24 for NELLCOR GR101704 manufactured by Nellcor Puritan Bennett Ireland.

Event Text Entries

[180754376] If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[180754377] According to the reporter, during use, the unit had a very high reading. It was stated that the pulse reading was 187. There was no patient harm.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number8020893-2020-00030
MDR Report Key9747135
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-02-24
Date of Report2020-02-24
Date of Event2020-02-07
Date Mfgr Received2020-02-07
Device Manufacturer Date2014-11-06
Date Added to Maude2020-02-24
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationBIOMEDICAL ENGINEER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactAVI KLUGER
Manufacturer Street5920 LONGBOW DRIVE
Manufacturer CityBOULDER CO 80301
Manufacturer CountryUS
Manufacturer Postal80301
Manufacturer Phone3035306582
Manufacturer G1NELLCOR PURITAN BENNETT IRELAND
Manufacturer StreetMICHEAL COLLINS RD MERVUE
Manufacturer CityGALWAY
Manufacturer CountryIE
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameNELLCOR
Generic NameOXIMETER
Product CodeDQA
Date Received2020-02-24
Model NumberGR101704
Catalog NumberGR101704
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerNELLCOR PURITAN BENNETT IRELAND
Manufacturer AddressMICHEAL COLLINS RD MERVUE GALWAY IE


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-24

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.