VIDAS? CA 15-3 ASSAY 30429

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 2018-07-05 for VIDAS? CA 15-3 ASSAY 30429 manufactured by Biomerieux, S.a..

Event Text Entries

[113273805] A customer in (b)(6) reported discrepant results for a patient's samples in association with the vidas? Ca 15-3 assay. On (b)(6) 2018 results: vidas? Test result: 33. 68 iu/ml. Roche test: 88. 90 iu/ml. On (b)(6) 2018 results: vidas? Test: 43. 28 iu/ml. On (b)(6) 2018 results: vidas? Test: 41. 98 iu/ml. Roche test: 64. 20 iu/ml. The customer stated the incorrect result was reported to the clinician, and that the result affected patient treatment. The customer stated that there was a misdiagnosis and they thought the patient was doing better when in fact the patient was not doing better. 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 Number3002769706-2018-00095
MDR Report Key7664538
Report SourceFOREIGN,HEALTH PROFESSIONAL,U
Date Received2018-07-05
Date of Report2018-08-30
Date Mfgr Received2018-08-03
Device Manufacturer Date2017-10-13
Date Added to Maude2018-07-05
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. TIFFANY HALL
Manufacturer Street100 RODOLPHE STREET
Manufacturer CityDURHAM NC 27712
Manufacturer CountryUS
Manufacturer Postal27712
Manufacturer G1BIOMERIEUX, S.A.
Manufacturer StreetCHEMIN DE L ORME
Manufacturer CityMARCY L ETOILE, RHONE 69280
Manufacturer CountryFR
Manufacturer Postal Code69280
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameVIDAS? CA 15-3 ASSAY
Generic NameVIDAS? CA 15-3 ASSAY
Product CodeLTK
Date Received2018-07-05
Catalog Number30429
Lot Number1006022590
Device Expiration Date2018-09-30
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBIOMERIEUX, S.A.
Manufacturer AddressCHEMIN DE L ORME MARCY L ETOILE, RHONE 69280 FR 69280


Patients

Patient NumberTreatmentOutcomeDate
10 2018-07-05

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