IMMULITE 2000 XPI CALCITONIN L5KCL

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 2010-06-15 for IMMULITE 2000 XPI CALCITONIN L5KCL manufactured by Siemens Healthcare Diagnostics Inc..

Event Text Entries

[1622813] A discordant low immulite 2000 xpi calcitonin result was obtained on a pt sample. The customer performed repeat calcitonin testing and the result was elevated. The discordant result was not reported to the physician. There was no report of pt treatment being altered or adverse health consequences due to the discordant low calcitonin assay result.
Patient Sequence No: 1, Text Type: D, B5


[8621651] A siemens field service engineer (fse) was sent to the customer site and performed a system eval. The fse was not able to determine the cause for the discordant low calcitonin result. The instrument is performing within specs.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number2017183-2010-00027
MDR Report Key1728315
Report Source05,06
Date Received2010-06-15
Date of Report2010-05-25
Date of Event2010-05-12
Date Mfgr Received2010-01-11
Date Added to Maude2011-04-18
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 FDA0
Event Location0
Manufacturer ContactSTEVEN ANDBERG
Manufacturer Street5210 PACIFIC CONCOURSE
Manufacturer CityLOS ANGELES CA 900455597
Manufacturer CountryUS
Manufacturer Postal900455597
Manufacturer Phone5086608540
Manufacturer G1SIEMENS HEALTHCARE DIAGNOSTICS, INC.
Manufacturer Street5700 WEST 96TH ST.
Manufacturer CityLOS ANGELES CA 90045559
Manufacturer CountryUS
Manufacturer Postal Code90045 5597
Single Use3
Remedial ActionOT
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameIMMULITE 2000 XPI CALCITONIN
Generic NameCALCITONIN IMMUNOASSAY
Product CodeJKR
Date Received2010-06-15
Model NumberNA
Catalog NumberL5KCL
Lot Number214
ID NumberNA
Device Expiration Date2010-10-31
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeNA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSIEMENS HEALTHCARE DIAGNOSTICS INC.
Manufacturer AddressLOS ANGELES CA US


Patients

Patient NumberTreatmentOutcomeDate
10 2010-06-15

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