VERITI DX THERMAL CYCLER 4452300

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,04,07 report with the FDA on 2014-03-25 for VERITI DX THERMAL CYCLER 4452300 manufactured by Life Technologies Holdings Pte. Ltd..

Event Text Entries

[4453945] A customer reported an error message "error 0x006" coming from the instrument, veriti dx thermal cycler (cat no. 4452300, serial no. (b)(4)). No pt involvement reported. (b)(4).
Patient Sequence No: 1, Text Type: D, B5


[11894326] Device is an instrument and it not implanted/explanted. The instrument was returned to life technologies corp and repaired by replacing the power amp board. After repair, unit functional test was performed and the instrument works as normal and the overall result is ok. Investigation is in process. Device intended use: the applied biosystems veriti dx thermal cycler amplifies human nucleic acid samples for diagnostic applications. The veriti dx thermal cycler is to be used only by operators trained in laboratory techniques and procedures.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number3003673482-2014-00006
MDR Report Key3835034
Report Source01,04,07
Date Received2014-03-25
Date of Report2014-02-25
Date of Event2014-02-25
Date Mfgr Received2014-02-25
Device Manufacturer Date2012-07-01
Date Added to Maude2014-06-13
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 ContactKELLI TANZELLA
Manufacturer Street3175 STALEY RD
Manufacturer CityGRAND ISLAND NY 14072
Manufacturer CountryUS
Manufacturer Postal14072
Manufacturer Phone7167743122
Manufacturer G1LIFE TECHNOLOGIES HOLDINGDS PTE. LTD.
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameVERITI DX THERMAL CYCLER
Product CodeNSU
Date Received2014-03-25
Catalog Number4452300
Lot Number299120179
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerLIFE TECHNOLOGIES HOLDINGS PTE. LTD.
Manufacturer AddressSN


Patients

Patient NumberTreatmentOutcomeDate
10 2014-03-25

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