VIDAS VARICELLA-ZOSTER IGG 30217

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,02,05 report with the FDA on 2015-04-08 for VIDAS VARICELLA-ZOSTER IGG 30217 manufactured by Biomerieux, S.a..

Event Text Entries

[20780848] On (b)(6) 2015 biom? Rieux received a complaint about false negative results obtained while using the vidas varicella-zoster igg. Vidas varicella-zoster igg (vzg) is an automated qualitative test for use on the instruments of the vidas family, for the detection of igg antibodies to varicella zoster virus in human serum using the elfa (enzyme linked fluorescent assay) technique. Vidas vzg is intended as an aid in the determination of immunological experience with varicella zoster virus. The customer performed a study comparing the vidas vzg test to the alegria test (manufactured by launch diagnostics). The study was performed by retesting twenty-three (23) stored blood samples of seventeen (17) pregnant women who had come in contact with the varicella-zoster virus from 2008 through 2014. The vidas vzg test reported twenty-one (21) negative results and two (2) equivocal results. The alegria test reported nine (9) positive results, two (2) negative results and twelve (12) equivocal results. The vidas result was reported to the physician, and the patient received immunoglobulin treatment. No adverse patient consequence was reported as a result of the treatment provided. As part of biomerieux's investigation, three (3) different lots (1003256630 exp. Date: 20-apr-2015, 1003490770 exp. Date: 27-jul-2015 and 1003778670 exp. Date: 24-nov-2015) from various points within their shelf-life were used to perform testing. Ten (10) samples known to give positive or equivocal results for the varicella virus were tested on each of the retained lots. The samples tested positive or equivocal results, as expected. Based on the results of the investigation, vidas varicella-zoster igg remains within the performance claims of the product.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3002769706-2015-00011
MDR Report Key4666935
Report Source01,02,05
Date Received2015-04-08
Date of Report2015-04-08
Date of Event2015-03-18
Date Mfgr Received2015-03-19
Date Added to Maude2015-04-08
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactMR. RYAN LEMELLE
Manufacturer Street595 ANGLUM ROAD
Manufacturer CityST. LOUIS MO 63042
Manufacturer CountryUS
Manufacturer Postal63042
Manufacturer Phone3147318582
Manufacturer G1BIOMERIEUX, S.A
Manufacturer Street5 RUE DE ACQUEDUCS
Manufacturer CityCRAPONNE, RHONE 69290
Manufacturer CountryFR
Manufacturer Postal Code69290
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameVIDAS VARICELLA-ZOSTER IGG
Generic NameENZYME LINKED IMMUNOABSORBENT ASSAY, VARICELLA-ZOSTER
Product CodeLFY
Date Received2015-04-08
Catalog Number30217
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBIOMERIEUX, S.A.
Manufacturer Address5 RUE DE ACQUEDUCS CRAPPONE, RHONE 69290 FR 69290


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2015-04-08

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