VITROS CHEMISTRY PRODUCTS LACTATE SLIDES 8150112

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-03-04 for VITROS CHEMISTRY PRODUCTS LACTATE SLIDES 8150112 manufactured by Ortho-clinical Diagnostics.

Event Text Entries

[141241500] The investigation determined that higher than expected vitros lac results were obtained from two different levels of non-vitros biorad multiqual unassayed control lot 47970, tested with vitros lac slide lot 3530-0103-5136 on a vitros 5600 integrated system. The investigation could not determine an assignable cause. The event suddenly occurred on (b)(6) 2019. Both acceptable and unacceptable vitros lac quality control results were obtained from two different affected cartridges, indicating the vitros lac slides in use did not likely contribute to the event. In addition, acceptable quality control results were obtained for 8 days prior to the event, using the same calibration event, indicating the event was not calibration driven. Acceptable quality control results were obtained after the event occurred, through the present, with no actions taken to improve performance. This indicates that vitros lac slide lot 3530-0103-5136 was performing as intended on the vitros 5600 integrated system since the event that occurred on (b)(6) 2019. Continual tracking and trending of complaints has not identified any signals that would point to a potential systemic issue with vitros lac slide lot 3530-0103-5136.
Patient Sequence No: 1, Text Type: N, H10


[141241501] A customer reported higher than expected quality control (qc) results obtained using vitros chemistry products lactate (lac) slides on a vitros 5600 integrated system. Non-vitros biorad quality control lot 47970. L1 vitros lac result of 2. 10 mmol/l vs. The expected result of 1. 43 mmol/l. L2 vitros lac results of 4. 43, 4. 44, and 4. 41 mmol/l vs. The expected result of 3. 49 mmol/l. 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 lac results were generated from non-patient fluids and the customer made no indication that patient samples were affected. There was no allegation of patient harm as a result of the event. This report is number 1 of 4 mdr? S for this event. Four (4) 3500a forms are being submitted for this event as 4 devices were involved. This report corresponds to ortho clinical diagnostics inc. Complaint number (b)(4).
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1319809-2019-00009
MDR Report Key8387354
Date Received2019-03-04
Date of Report2019-03-04
Date of Event2019-01-18
Date Mfgr Received2019-02-06
Device Manufacturer Date2018-11-30
Date Added to Maude2019-03-04
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 ContactMR. JAMES A STEVENS
Manufacturer Street100 INDIGO CREEK DRIVE
Manufacturer CityROCHESTER NY 14626
Manufacturer CountryUS
Manufacturer Postal14626
Manufacturer Phone5854533000
Manufacturer G1ORTHO-CLINICAL DIAGNOSTICS
Manufacturer Street513 TECHNOLOGY BLVD.
Manufacturer CityROCHESTER NY 14652
Manufacturer CountryUS
Manufacturer Postal Code14652
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameVITROS CHEMISTRY PRODUCTS LACTATE SLIDES
Generic NameIN VITRO DIAGNOSTICS
Product CodeKHP
Date Received2019-03-04
Catalog Number8150112
Lot Number3530-0103-5136
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 2019-03-04

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