VITROS 5600 INTEGRATED SYSTEM 6801042

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-06-23 for VITROS 5600 INTEGRATED SYSTEM 6801042 manufactured by Ortho-clinical Diagnostics.

Event Text Entries

[78397230] The investigation determined that lower than expected myoglobin results were obtained from two levels of biorad quality control fluids processed using vitros myoglobin reagent on a vitros 5600 integrated system. The most likely assignable cause is instrument related. A review of historical biorad qc fluid performance across two vitros 5600 systems in the laboratory concluded that myoglobin imprecision was occurring on only one vitros system suggesting that the issue is most likely instrument and not reagent related. An ortho field engineer performed service actions that include replacement of the reagent metering probe and adjustments in several subsystems. Following these actions, acceptable within run myoglobin precision results were obtained. In addition, acceptable biorad qc performance was maintained indicating the vitros 5600 system was performing as expected following service actions.
Patient Sequence No: 1, Text Type: N, H10


[78397231] The investigation determined that lower than expected myoglobin results were obtained from two levels of non-vitros biorad lot 23630 quality control fluids processed using vitros immunodiagnostics products myoglobin reagent lot 1210 on a vitros 5600 integrated system. Biorad level 1= 101. 4, 89. 63, 113. 46, 110. 188, 116. 413, 113. 041, 118. 559, 78. 998, 82. 18, 109. 92, 116. 995, 95. 58, 93. 59, 96. 5, 96. 312, 82. 75, 84. 98 and 96. 67 ng/ml versus expected 131 ng/ml. Biorad level 2= 0. 90 and 91. 096 ng/ml versus expected 251 ng/ml. Biased results of the magnitude and direction observed may lead to inappropriate physician action if they were to occur undetected on patient samples. The unexpected vitros myoglobin results were generated from non-patient fluids, however the investigation cannot conclude that patient sample results were not affected and would not be affected if the event were to recur undetected. There was no allegation of patient harm as a result of the event. This report corresponds to ortho clinical diagnostics inc. Complaint number (b)(4).
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1319681-2017-00047
MDR Report Key6662840
Date Received2017-06-23
Date of Report2017-06-23
Date of Event2017-05-28
Date Mfgr Received2017-05-28
Device Manufacturer Date2017-01-04
Date Added to Maude2017-06-23
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag0
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. JAMES A STEVENS
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 Report0

Device Sequence Number: 0

Brand NameVITROS 5600 INTEGRATED SYSTEM
Generic NameCHEMISTRY ANALYZER
Product CodeDDR
Date Received2017-06-23
Catalog Number6801042
Device Expiration Date2017-11-13
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrY
Device Sequence No0
Device Event Key0
ManufacturerORTHO-CLINICAL DIAGNOSTICS
Manufacturer Address100 INDIGO CREEK DRIVE ROCHESTER NY 14626 US 14626

Device Sequence Number: 1

Brand NameVITROS 5600 INTEGRATED SYSTEM
Generic NameCHEMISTRY ANALYZER
Product CodeJJE
Date Received2017-06-23
Catalog Number6801042
Device Expiration Date2017-11-13
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 2017-06-23

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