VIDAS? LYME IGM 416436

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2017-12-01 for VIDAS? LYME IGM 416436 manufactured by Biomerieux Sa.

Event Text Entries

[94737638] A customer from the united states notified biom? Rieux of false negative results associated with the vidas? Lyme igm involving a patient sample. The customer indicated running the patient sample and getting negative result; however, the sample was sent to a reference lab where the western blot was positive for multiple bands. The customer reported the specimen they tested and the specimen the reference lab tested were obtained from the patient at the same time but were in different tubes. Serum was used for both tests. The customer indicated neither specimen is available for submission to biom? Rieux.. A biom? Rieux investigation will be initiated.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3002769706-2017-00391
MDR Report Key7076035
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2017-12-01
Date of Report2018-03-02
Date Mfgr Received2018-02-06
Device Manufacturer Date2017-04-21
Date Added to Maude2017-12-01
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. ELLEN WELTMER
Manufacturer Street595 ANGLUM ROAD
Manufacturer CityST. LOUIS MO 63042
Manufacturer CountryUS
Manufacturer Postal63042
Manufacturer G1BIOMERIEUX SA
Manufacturer StreetCHEMIN DE L ORME MARCY L ETOILE, RHONE 69280
Manufacturer CountryFR
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameVIDAS? LYME IGM
Generic NameVIDAS? LYME IGM
Product CodeLSR
Date Received2017-12-01
Catalog Number416436
Lot Number1005662400
Device Expiration Date2018-07-08
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 2017-12-01

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