RAD-97 W/NIBP 26038 9797

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-17 for RAD-97 W/NIBP 26038 9797 manufactured by Masimo - 52 Discovery.

Event Text Entries

[183896464] The product has been returned to the local facility but has not yet been received at the main office for evaluation. Once returned and investigated, a follow-up report will be submitted.
Patient Sequence No: 1, Text Type: N, H10


[183896465] The customer reported that the device stops by itself. No consequences or impact to patient were reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3011353843-2020-00038
MDR Report Key9842098
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-03-17
Date of Report2020-02-20
Date of Event1901-01-01
Date Mfgr Received2020-02-20
Device Manufacturer Date2017-03-24
Date Added to Maude2020-03-17
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactSTEFAN LISSMANN
Manufacturer Street52 DISCOVERY
Manufacturer CityIRVINE CA 92618
Manufacturer CountryUS
Manufacturer Postal92618
Manufacturer Phone9492977168
Manufacturer G1MASIMO - MEXICALI
Manufacturer StreetINDUSTRIAL VALLERA DE MEXICALI CALZADA DEL ORO, NO.2001
Manufacturer CityMEXICALI, BAJA CALIFORNIA 21600
Manufacturer CountryMX
Manufacturer Postal Code21600
Single Use3
Remedial ActionOT
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameRAD-97 W/NIBP
Generic NameOXIMETER
Product CodeMWI
Date Received2020-03-17
Returned To Mfg2020-03-06
Model Number26038
Catalog Number9797
Device AvailabilityR
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerMASIMO - 52 DISCOVERY
Manufacturer Address52 DISCOVERY IRVINE CA 92618 US 92618


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-17

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