VIDAS? LYME IGG 30320

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,u report with the FDA on 2018-10-09 for VIDAS? LYME IGG 30320 manufactured by Biomerieux Sa.

Event Text Entries

[123849231] A customer in (b)(6) reported a false negative result in association with vidas? Lyme igg (1006179040). The customer reported that while comparing test results for four patient samples on two different lots, there was a change of interpretation from positive to negative with lot 1006179040, for one patient sample. This customer reported this sample was tested in wb: positive vlse, p41 positive and p18 positive, and had a lyme m negative test. There is no indication or report from the hospital or treating physician to biom? Rieux that the discrepant result led to any adverse event related to the patient's state of health. A biom? Rieux internal investigation will be initiated.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3002769706-2018-00205
MDR Report Key7948438
Report SourceFOREIGN,HEALTH PROFESSIONAL,U
Date Received2018-10-09
Date of Report2018-10-09
Date Mfgr Received2018-09-09
Device Manufacturer Date2017-12-21
Date Added to Maude2018-10-09
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 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 Report3

Device Details

Brand NameVIDAS? LYME IGG
Generic NameVIDAS? LYME IGG
Product CodeLSR
Date Received2018-10-09
Catalog Number30320
Lot Number1006179040
Device Expiration Date2018-11-25
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
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 2018-10-09

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