URISYS 1100 03617556001

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,other report with the FDA on 2015-11-10 for URISYS 1100 03617556001 manufactured by Roche Diagnostics.

Event Text Entries

[30873375]
Patient Sequence No: 1, Text Type: N, H10


[30873376] Reporter stated that the urisys 1100 reported negative results for leukocytes, while visual read of test strips showed values of 500 leukocytes/microliter. No adverse event was reported. The manufacturer requested the return of the suspect product for evaluation.
Patient Sequence No: 1, Text Type: D, B5


[35021643] The customer did not return the urisys 1100 device so it could not be investigated. The urisys 1000 device was not returned.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1823260-2015-04500
MDR Report Key5213873
Report SourceCOMPANY REPRESENTATIVE,OTHER
Date Received2015-11-10
Date of Report2016-01-05
Date of Event2015-10-01
Date Mfgr Received2015-10-14
Date Added to Maude2015-11-10
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationMEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactNA MICHAEL LESLIE
Manufacturer Street9115 HAGUE ROAD NA
Manufacturer CityINDIANAPOLIS IN 46250
Manufacturer CountryUS
Manufacturer Postal46250
Manufacturer Phone3175214343
Manufacturer G1ROCHE DIAGNOSTICS GMBH
Manufacturer StreetSANDHOFERSTRASSE 116 NA
Manufacturer CityMANNHEIM (BADEN-WURTTEMBERG) 68305
Manufacturer CountryGM
Manufacturer Postal Code68305
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameURISYS 1100
Generic NameAUTOMATED URINE ANALYZER
Product CodeKHE
Date Received2015-11-10
Model NumberNA
Catalog Number03617556001
Lot NumberNA
ID NumberNA
OperatorNURSE
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerROCHE DIAGNOSTICS
Manufacturer Address9115 HAGUE ROAD NA INDIANAPOLIS IN 46250 US 46250


Patients

Patient NumberTreatmentOutcomeDate
10 2015-11-10

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