ELECSYS T4 ASSAY

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-01-29 for ELECSYS T4 ASSAY manufactured by Roche Diagnostics.

Event Text Entries

[134470884] The investigation did not identify a product problem. As insufficient patient sample material remained, the cause of the event could not be determined. From the information provided, a general reagent issue could most likely be excluded. No devices were returned. This device is not labeled for single use and is not reprocessed or reused.
Patient Sequence No: 1, Text Type: N, H10


[134470925] This report summarizes 1 malfunction events. Erroneous high elecsys t4 assay results were generated. The events involved 1 patient. The patient's age was (b)(6). The patient's weight was requested but was not provided. The patient was female. The patient's race was requested but was not provided. The patient's ethnicity was requested but was not provided.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1823260-2019-90071
MDR Report Key8285294
Date Received2019-01-29
Date Added to Maude2019-01-29
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA0
Report to FDA3
Event Location3
Manufacturer ContactMICHAEL LESLIE
Manufacturer Street9115 HAGUE ROAD NA
Manufacturer CityINDIANAPOLIS IN 46250
Manufacturer CountryUS
Manufacturer Postal46250
Manufacturer Phone3175214343
Manufacturer G1ROCHE DIAGNOSTICS GMBH
Manufacturer StreetSANDHOFFERSTRASSE 116 NA
Manufacturer CityMANNHEIM (BADEN-WURTTEMBERG), NA 68305
Manufacturer CountryGM
Manufacturer Postal Code68305
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameELECSYS T4 ASSAY
Generic NameRADIOIMMUNOASSAY, TOTAL THYROXINE
Product CodeCDX
Date Received2019-01-29
Model NumberT4
Lot NumberASKU
Device Availability*
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerROCHE DIAGNOSTICS
Manufacturer Address9115 HAGUE ROAD NA INDIANAPOLIS IN 46250 US 46250


Patients

Patient NumberTreatmentOutcomeDate
10 2019-01-29

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