BILT3 BILIRUBIN TOTAL GEN.3 05795397190

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,u report with the FDA on 2018-08-13 for BILT3 BILIRUBIN TOTAL GEN.3 05795397190 manufactured by Roche Diagnostics.

Event Text Entries

[117289476] (b)(6).
Patient Sequence No: 1, Text Type: N, H10


[117289477] The customer complained of discrepant bilt3 bilirubin total gen. 3 results for 2 infants that were twins on a cobas 6000 c (501) module compared to a advanced bilirubin stat-analyzer model br-2. The c 501 serial number was (b)(4). There was no allegation of an adverse event. The initial investigation determined that the calibration was acceptable.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1823260-2018-02711
MDR Report Key7778101
Report SourceFOREIGN,HEALTH PROFESSIONAL,U
Date Received2018-08-13
Date of Report2018-09-26
Date of Event2018-07-24
Date Mfgr Received2018-07-26
Date Added to Maude2018-08-13
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 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 NameBILT3 BILIRUBIN TOTAL GEN.3
Generic NameDIAZO COLORIMETRY, BILIRUBIN
Product CodeCIG
Date Received2018-08-13
Model NumberNA
Catalog Number05795397190
Lot Number281255
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerROCHE DIAGNOSTICS
Manufacturer Address9115 HAGUE ROAD NA INDIANAPOLIS IN 462500457 US 462500457


Patients

Patient NumberTreatmentOutcomeDate
10 2018-08-13

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