VITROS 5600 INTEGRATED SYSTEM 6802413

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2012-12-17 for VITROS 5600 INTEGRATED SYSTEM 6802413 manufactured by Ortho-clinical Diagnostics.

Event Text Entries

[3180129] The customer obtained a non-reproducible, higher than expected vitros ckmb result (52. 4 vs. An expected result= 2. 37 ng/ml) from a single patient sample run on the vitros 5600 integrated system. Biased results of the magnitude and direction observed may lead to inappropriate physician action. However, the higher than expected result was questioned and repeated due to patient history, prior to reporting out of the laboratory. There was no report of patient harm as a result of this event. (b)(4).
Patient Sequence No: 1, Text Type: D, B5


[10533827] The investigation determined that a non-reproducible, higher than expected vitros ckmb result was obtained from a single patient sample run on the vitros 5600 integrated system. There was no evidence to suggest an instrument or reagent related issue contributed to the event. Root cause of the event could not be determined, however, it is likely that contamination within the vitros 5600 system had contributed to the results. Additionally, poor sample processing or a sample mix-up cannot be ruled out as contributing factors.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1319681-2012-00241
MDR Report Key2876436
Report Source05
Date Received2012-12-17
Date of Report2012-12-17
Date of Event2012-11-17
Date Mfgr Received2012-11-18
Device Manufacturer Date2011-04-28
Date Added to Maude2013-03-20
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationMEDICAL TECHNOLOGIST
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactMR. JOSEPH FALVO
Manufacturer Street100 INDIGO CREEK DRIVE
Manufacturer CityROCHESTER NY 14626
Manufacturer CountryUS
Manufacturer Postal14626
Manufacturer Phone5854533000
Manufacturer G1ORTHO-CLINICAL DIAGNOSTICS
Manufacturer Street100 INDIGO CREEK DRIVE
Manufacturer CityROCHESTER NY 14626
Manufacturer CountryUS
Manufacturer Postal Code14626
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameVITROS 5600 INTEGRATED SYSTEM
Generic NameCHEMISTRY ANALYZER
Product CodeJLB
Date Received2012-12-17
Catalog Number6802413
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerORTHO-CLINICAL DIAGNOSTICS
Manufacturer Address100 INDIGO CREEK DRIVE ROCHESTER NY 14626 US 14626


Patients

Patient NumberTreatmentOutcomeDate
10 2012-12-17

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