NOVA STAT PROFILE PHOX ULTRA 42014

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-01-11 for NOVA STAT PROFILE PHOX ULTRA 42014 manufactured by Nova Biomedical Corporation.

Event Text Entries

[134732775] No adverse event or patient impact was reported. Investigation ongoing.
Patient Sequence No: 1, Text Type: N, H10


[134732776] On (b)(6) 2018: discrepant creatinine results for patient in cancer center when compared to lab.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1219029-2019-00002
MDR Report Key8241359
Date Received2019-01-11
Date of Report2019-01-11
Date of Event2018-09-26
Date Mfgr Received2018-12-13
Date Added to Maude2019-01-11
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. TAYLOR WARD
Manufacturer Street200 PROSPECT ST
Manufacturer CityWALTHAM MA 024543465
Manufacturer CountryUS
Manufacturer Postal024543465
Manufacturer Phone7816473700
Manufacturer G1NOVA BIOMEDICAL CORPORATION
Manufacturer Street200 PROSPECT STREET
Manufacturer CityWALTHAM MA 024543465
Manufacturer CountryUS
Manufacturer Postal Code024543465
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameNOVA STAT PROFILE PHOX ULTRA
Generic NameELECTRODE, ION BASED, ENZYMATIC, CREATININE
Product CodeCGL
Date Received2019-01-11
Model Number42014
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerNOVA BIOMEDICAL CORPORATION
Manufacturer Address200 PROSPECT STREET WALTHAM MA 024543465 US 024543465


Patients

Patient NumberTreatmentOutcomeDate
10 2019-01-11

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