VIDAS? TOXO IGM 30202

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 2016-12-15 for VIDAS? TOXO IGM 30202 manufactured by Biomerieux Sa.

Event Text Entries

[62692691] A customer in (b)(6) reported to biom? Rieux that they have observed false negative results, as part of eqa toxo 163, in association with the vidas? Toxo igm test. The customer indicated the serum is a known positive and the test results were: 0. 49 => negative. An internal biom? Rieux investigation was conducted. The complaint is about the (b)(6) eqa toxo 163 from ctcb (centre toulousain pour le contr? Le de qualit? En biologie clinique) found negative by the majority of participants whereas it was expected to be positive with vidas? Toxo igm reference (b)(4). Results for this control ctcb toxo 163 are as follows : (b)(6) participants gave a positive result as expected, (b)(6) participants gave an equivocal result, (b)(6) participants gave a negative result. The study of batch history record for vidas? Toxo igm lots 1004881890 / 170306-0 shows no anomaly during the control process. The quality product laboratory observed control charts for 5 internal samples from quality control department for 6 lots of vidas? Toxo igm. All the results are within expected ranges and all batches are within the trend of the parameter. Quality product department tested the control ctcb toxo 163 and found an equivocal result on a different vidas? Toxo igm lot. Quality product department confirms results indicated in ctcb report. Complementary results are indicated in ctcb report for control ctcb toxo 163 : vidas? Toxo igg ii : 95 ui/ml positive (pre-testing result), vidas? Toxo igg avidity : 0410 tv high (pre-testing result), toxo isaga positive (result found by 12/12 participants). An result of avidity higher than 0. 300 indicates an old infection, older than 4 months. Quality product conclude to a probable old infection for control ctcb toxo 163. This control could contain residual igm which are not detected by vidas? Technique. This conclusion matches with the conclusion proposed by the ctcb in the report. Vidas? Toxo igm lots1004881890 / 170306-0 performed as expected. An anomaly was linked to the control ctcb toxo 163 which probably contains residual igm.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3002769706-2016-00514
MDR Report Key6177580
Report SourceFOREIGN,HEALTH PROFESSIONAL,U
Date Received2016-12-15
Date of Report2016-11-22
Date Mfgr Received2016-11-22
Date Added to Maude2016-12-15
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 ContactMRS. ELLEN WELTMER
Manufacturer Street595 ANGLUM ROAD
Manufacturer CityHAZELWOOD MO 63042
Manufacturer CountryUS
Manufacturer Postal63042
Manufacturer Phone3147317301
Manufacturer G1BIOMERIEUX SA
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? TOXO IGM
Generic NameVIDAS? TOXO IGM
Product CodeLYR
Date Received2016-12-15
Catalog Number30202
Lot Number1004881890
Device Expiration Date2017-03-06
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 69280


Patients

Patient NumberTreatmentOutcomeDate
10 2016-12-15

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