BARD? CRITICORE? MONITOR 000002N

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-12-04 for BARD? CRITICORE? MONITOR 000002N manufactured by Medivance, Inc. ? 1725056.

Event Text Entries

[129754675] The investigation is still in progress. Once the investigation is complete a supplemental report will be filed.
Patient Sequence No: 1, Text Type: N, H10


[129754676] It was reported that the criticore monitor was not reading the urine volume.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1018233-2018-05801
MDR Report Key8130652
Date Received2018-12-04
Date of Report2019-01-18
Date Mfgr Received2019-01-07
Date Added to Maude2018-12-04
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 ContactYONIC ANDERSON
Manufacturer Street8195 INDUSTRIAL BLVD
Manufacturer CityCOVINGTON GA 30014
Manufacturer CountryUS
Manufacturer Postal30014
Manufacturer Phone7707846100
Manufacturer G1MEDIVANCE, INC.
Manufacturer Street321 S TAYLOR AVE
Manufacturer CityLOUISVILLE CO 80027
Manufacturer CountryUS
Manufacturer Postal Code80027
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameBARD? CRITICORE? MONITOR
Generic NameCRITICORE MONITOR
Product CodeEXS
Date Received2018-12-04
Returned To Mfg2018-11-21
Model Number000002N
Catalog Number000002N
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerMEDIVANCE, INC. ? 1725056
Manufacturer Address321 S TAYLOR AVE LOUISVILLE CO 80027 US 80027


Patients

Patient NumberTreatmentOutcomeDate
10 2018-12-04

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