MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-02-08 for VIDAS? RUB IGG 30221 manufactured by Biomerieux Sa.
[136284195]
A customer in the united states reported a false negative result for a (b)(6) survey sample in association with the vidas? Rubella (rub) igg assay. The customer stated they reported that rub igg antibodies were absent (negative) with a result of 9 ui/ml. The expected result was rub igg antibodies present (positive). A biom? Rieux internal investigation will be initiated.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 8020790-2019-00011 |
MDR Report Key | 8322678 |
Date Received | 2019-02-08 |
Date of Report | 2019-05-27 |
Date Mfgr Received | 2019-05-03 |
Device Manufacturer Date | 2018-06-01 |
Date Added to Maude | 2019-02-08 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Health Professional | 0 |
Initial Report to FDA | 0 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MS. DEBRA BROYLES |
Manufacturer Street | 595 ANGLUM ROAD |
Manufacturer City | HAZELWOOD MO 63042 |
Manufacturer Country | US |
Manufacturer Postal | 63042 |
Manufacturer G1 | BIOMERIEUX SA |
Manufacturer Street | CHEMIN DE L ORME |
Manufacturer City | MARCY L ETOILE, RHONE 69280, |
Manufacturer Country | FR |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | VIDAS? RUB IGG |
Generic Name | VIDAS? RUB IGG |
Product Code | LFX |
Date Received | 2019-02-08 |
Catalog Number | 30221 |
Lot Number | 1006549030 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BIOMERIEUX SA |
Manufacturer Address | CHEMIN DE L ORME MARCY L ETOILE, RHONE 69280, FR |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-02-08 |