IMMUNOGLOBULIN E 04827031190

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 2016-01-26 for IMMUNOGLOBULIN E 04827031190 manufactured by Roche Diagnostics.

Event Text Entries

[36806824] This event occurred in (b)(6).
Patient Sequence No: 1, Text Type: N, H10


[36806825] The customer complained of erroneous results for 1 patient sample tested for immunoglobulin e (ige ii). It is not known if erroneous results were reported outside of the laboratory. The initial ige ii result from the modular e analyzer was 106350 ku/l. The repeat result from a siemens centaur instrument was 420 ku/l. The ige from an electrophoresis was normal. No adverse event occurred. The modular e analyzer serial number was (b)(4). It was noted that liquid flow cleaning is performed every 2 weeks.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1823260-2016-00074
MDR Report Key5390208
Report SourceFOREIGN,HEALTH PROFESSIONAL,U
Date Received2016-01-26
Date of Report2016-01-26
Date of Event2015-12-24
Date Mfgr Received2016-01-11
Date Added to Maude2016-01-26
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 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
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 NameIMMUNOGLOBULIN E
Generic NameRADIOIMMUNOASSAY, IMMUNOGLOBULINS (D, E)
Product CodeJHR
Date Received2016-01-26
Model NumberNA
Catalog Number04827031190
Lot Number188637
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
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 2016-01-26

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