ANTI-FYB (ANTI-DUFFY) FOR INDIRECT ANTIGLOBULIN TEST NI 103076

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 2003-05-15 for ANTI-FYB (ANTI-DUFFY) FOR INDIRECT ANTIGLOBULIN TEST NI 103076 manufactured by Ortho-clinical Diagnostics.

Event Text Entries

[274305] Customer reported that negative reactions were observed with this lot of anti-fyb and several fyb+ cells. No death or serious injury was associated with this incident.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2250051-2003-00111
MDR Report Key461455
Report Source05
Date Received2003-05-15
Date of Report2003-05-12
Date of Event2003-04-17
Date Mfgr Received2003-04-17
Date Added to Maude2003-05-23
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 ContactNANCY PAPCIAK
Manufacturer Street1001 US HWY 202
Manufacturer CityRARITAN NJ 088690606
Manufacturer CountryUS
Manufacturer Postal088690606
Manufacturer Phone9087043872
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Remedial ActionOT
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameANTI-FYB (ANTI-DUFFY) FOR INDIRECT ANTIGLOBULIN TEST
Generic NameBLOOD GROUPING REAGENT
Product CodeLSE
Date Received2003-05-15
Model NumberNI
Catalog Number103076
Lot NumberFYB53A
ID NumberNA
Device Expiration Date2003-09-04
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key450397
ManufacturerORTHO-CLINICAL DIAGNOSTICS
Manufacturer Address1001 US HWY 202 RARITAN NJ 088690606 US
Baseline Brand NameANTI-FYB (ANTI-DUFFY) FOR INDIRECT ANTIGLOBULIN TEST
Baseline Generic NameBLOOD GROUPING REAGENT
Baseline Model NoNI
Baseline Catalog No103076
Baseline IDNA


Patients

Patient NumberTreatmentOutcomeDate
10 2003-05-15

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