IMMULITE 2000/IMMULITE 2000 XPI THYROGLOBULIN L2KTY2

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-11-17 for IMMULITE 2000/IMMULITE 2000 XPI THYROGLOBULIN L2KTY2 manufactured by Siemens Healthcare Diagnostics Products, Limited.

Event Text Entries

[93319703] Siemens is evaluating the issue.
Patient Sequence No: 1, Text Type: N, H10


[93319704] Siemens technical operations internal investigation has identified that discordant falsely low results were obtained on two investigational samples on an immulite 2000/ immulite 2000 xpi instrument when using the thyroglobulin assay. The two investigational samples were spiked with biotin at multiple concentrations and run for investigational purposes on an immulite 2000/immulite 2000 xpi instrument. The results of the two samples spiked with 19 ng/ml of biotin were falsely low with a bias of -35% and -33% respectively compared to results of the two samples without biotin. There were no patient samples impacted as this was for investigational purposes only.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2432235-2017-00615
MDR Report Key7041461
Date Received2017-11-17
Date of Report2017-12-19
Date of Event2017-10-26
Date Mfgr Received2017-12-18
Date Added to Maude2017-11-17
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 ContactAARTI AZIZ
Manufacturer Street511 BENEDICT AVENUE
Manufacturer CityTARRYTOWN NY 10591
Manufacturer CountryUS
Manufacturer Postal10591
Manufacturer Phone9145242683
Manufacturer G1SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, LIMITED
Manufacturer StreetUK REGISTRATION #: 3002806944 GLYN RHONWY
Manufacturer CityLLANBERIS, GWYNEDD LL554EL
Manufacturer CountryUK
Manufacturer Postal CodeLL55 4EL
Single Use3
Previous Use Code3
Removal Correction Number2432235-12/19/2017-004-C
Event Type3
Type of Report0

Device Details

Brand NameIMMULITE 2000/IMMULITE 2000 XPI THYROGLOBULIN
Generic NameIMMULITE 2000/IMMULITE 2000 XPI THYROGLOBULIN
Product CodeMSW
Date Received2017-11-17
Model NumberIMMULITE 2000/IMMULITE 2000 XPI THYROGLOBULIN
Catalog NumberL2KTY2
Lot Number355
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS, LIMITED
Manufacturer AddressGLYN RHONWY LLANBERIS, GWYNEDD LL554EL UK LL55 4EL


Patients

Patient NumberTreatmentOutcomeDate
10 2017-11-17

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