IMMULITE 2000 N/A 030002

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 2011-01-05 for IMMULITE 2000 N/A 030002 manufactured by Siemens Healthcare Diagnostics.

Event Text Entries

[18079926] A siemens fse (field service engineer) evaluated the immulite 2000 instrument data. Analysis of the instrument and instrument data indicate that the cause for the discordant sps result is unknown. The instrument is performing within specifications. No further evaluation of the device is required.
Patient Sequence No: 1, Text Type: N, H10


[18242774] Discordant immulite 2000 sps results were obtained on one (1) patient sample. The laboratory questioned the result and repeated the sample to confirm. The corrected result was reported to the physician. There was no report of adverse health consequences due to the discordant sps results.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2247117-2010-00058
MDR Report Key1948593
Report Source05,06
Date Received2011-01-05
Date of Report2010-12-09
Date of Event2010-12-03
Date Mfgr Received2010-12-09
Date Added to Maude2011-04-07
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 FDA0
Event Location0
Manufacturer ContactLINDA BARLETTA
Manufacturer Street511 BENEDICT AVENUE
Manufacturer CityTARRYTOWN NY 10591
Manufacturer CountryUS
Manufacturer Postal10591
Manufacturer Phone9145242299
Manufacturer G1SIEMENS HEALTHCARE DIAGNOSTICS
Manufacturer Street62 FLANDERS BARTLEY ROAD
Manufacturer CityFLANDERS NJ 07836
Manufacturer CountryUS
Manufacturer Postal Code07836
Single Use3
Remedial ActionOT
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameIMMULITE 2000
Generic NameIMMUNO-ASSAY
Product CodeDGC
Date Received2011-01-05
Model NumberN/A
Catalog Number030002
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSIEMENS HEALTHCARE DIAGNOSTICS
Manufacturer AddressFLANDERS NJ 07835 US 07835


Patients

Patient NumberTreatmentOutcomeDate
10 2011-01-05

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