Drug recall
VIDAS 3 software v. 1.1.4
FDA recall event 76281 · Class II · BioMerieux SA
Key facts
| Event ID | 76281 |
|---|---|
| Recall numbers | Z-1200-2017 |
| Recalling firm | BioMerieux SA |
| Product type | Devices |
| Products | VIDAS 3 software v. 1.1.4 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | During development of the VIDAS 3 software version 1.2, some anomalies have been identified and observed to be already present in the current software version VIDAS 3 version 1.1.4. available in the… |
| Initiation date | Jan 11, 2017 |
| Report date | Feb 22, 2017 |
| Termination date | Aug 28, 2017 |
| City | Marcy L'Etoile |
| Country | France |
| FEI number | 1000611339 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: