VITROS IMMUNODIAGNOSTIC PRODUCTS CKMB REAGENT PACK 1896836

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 2001-12-28 for VITROS IMMUNODIAGNOSTIC PRODUCTS CKMB REAGENT PACK 1896836 manufactured by Ortho-clinical Diagnostics.

Event Text Entries

[19955453] The customer obtained a false low ckmb result of 0. 30 ng/ml on 3 patient sample the same sample was repeated and the customer obtained results of 3710 ng/ml and 35. 40 ng/ml. The based low result was not reported to the physician. There was no report of patient harm as a result of this event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9680658-2001-00053
MDR Report Key369175
Report Source05
Date Received2001-12-28
Date of Report2001-11-28
Date of Event2001-10-21
Date Mfgr Received2001-11-28
Device Manufacturer Date2001-06-01
Date Added to Maude2002-01-03
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location0
Manufacturer ContactFRED LASKY
Manufacturer Street100 INDIGO CREEK DRIVE
Manufacturer CityROCHESTER NY 146265101
Manufacturer CountryUS
Manufacturer Postal146265101
Manufacturer Phone7164533880
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameVITROS IMMUNODIAGNOSTIC PRODUCTS CKMB REAGENT PACK
Generic NameIN VIRTO DIAGNOSTIC
Product CodeJHY
Date Received2001-12-28
Model NumberNA
Catalog Number1896836
Lot Number180
ID NumberNA
Device Expiration Date2001-12-31
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrY
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key358291
ManufacturerORTHO-CLINICAL DIAGNOSTICS
Manufacturer Address100 INDIGO CREEK DRIVE ROCHESTER NY 146265101 US
Baseline Brand NameVITROS IMMUNODIAGNOSTIC PRODUCTS CKMB REAGENT PACK
Baseline Generic NameIN VIRTO DIAGNOSTIC
Baseline Model NoNA
Baseline Catalog No1896836
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
10 2001-12-28

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.