VITROS CHEMISTRY PRODUCTS CKMB SLIDES 8058232

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05 report with the FDA on 2003-11-12 for VITROS CHEMISTRY PRODUCTS CKMB SLIDES 8058232 manufactured by Ortho-clinical Diagnostics.

Event Text Entries

[331544] The customer observed low qc results after calibrating for a new lot of ckmb slides. No patient samples were processed. The results were not reported to the physician. This event is consistent with a malfunction that could have caused biased results to be reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1319809-2003-00246
MDR Report Key495646
Report Source01,05
Date Received2003-11-12
Date of Report2003-10-15
Date of Event2003-10-15
Date Mfgr Received2003-10-15
Device Manufacturer Date2003-01-01
Date Added to Maude2003-11-18
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 Location0
Manufacturer ContactTHOMAS SMITH
Manufacturer Street100 INDIGO CREEK DRIVE
Manufacturer CityROCHESTER NY 146265101
Manufacturer CountryUS
Manufacturer Postal146265101
Manufacturer Phone5854533735
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameVITROS CHEMISTRY PRODUCTS CKMB SLIDES
Generic NameIN VITRO DIAGNOSTIC
Product CodeJHY
Date Received2003-11-12
Model NumberNA
Catalog Number8058232
Lot Number4914-5779
ID NumberNA
Device Expiration Date2004-06-01
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrY
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key484377
ManufacturerORTHO-CLINICAL DIAGNOSTICS
Manufacturer Address100 INDIGO CREEK DRIVE ROCHESTER NY 146265101 US
Baseline Brand NameVITROS CHEMISTRY PRODUCTS CKMB SLIDES
Baseline Generic NameIN VITRO DIAGNOSTIC
Baseline Model NoNA
Baseline Catalog No8058232
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
10 2003-11-12

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