VIDAS? RUB IGG 30221

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-02-08 for VIDAS? RUB IGG 30221 manufactured by Biomerieux Sa.

Event Text Entries

[136284195] A customer in the united states reported a false negative result for a (b)(6) survey sample in association with the vidas? Rubella (rub) igg assay. The customer stated they reported that rub igg antibodies were absent (negative) with a result of 9 ui/ml. The expected result was rub igg antibodies present (positive). A biom? Rieux internal investigation will be initiated.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number8020790-2019-00011
MDR Report Key8322678
Date Received2019-02-08
Date of Report2019-05-27
Date Mfgr Received2019-05-03
Device Manufacturer Date2018-06-01
Date Added to Maude2019-02-08
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional0
Initial Report to FDA0
Report to FDA3
Event Location3
Manufacturer ContactMS. DEBRA BROYLES
Manufacturer Street595 ANGLUM ROAD
Manufacturer CityHAZELWOOD MO 63042
Manufacturer CountryUS
Manufacturer Postal63042
Manufacturer G1BIOMERIEUX SA
Manufacturer StreetCHEMIN DE L ORME
Manufacturer CityMARCY L ETOILE, RHONE 69280,
Manufacturer CountryFR
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameVIDAS? RUB IGG
Generic NameVIDAS? RUB IGG
Product CodeLFX
Date Received2019-02-08
Catalog Number30221
Lot Number1006549030
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBIOMERIEUX SA
Manufacturer AddressCHEMIN DE L ORME MARCY L ETOILE, RHONE 69280, FR


Patients

Patient NumberTreatmentOutcomeDate
10 2019-02-08

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