Drug recall
bioM¿rieux VITEK 2 NH ID Test Kit Product Usage: Is an automated system consisting of instruments, software…
FDA recall event 80491 · Class II · Biomerieux Inc
Key facts
| Event ID | 80491 |
|---|---|
| Recall numbers | Z-2874-2018 |
| Recalling firm | Biomerieux Inc |
| Product type | Devices |
| Products | bioM¿rieux VITEK 2 NH ID Test Kit Product Usage: Is an automated system consisting of instruments, software and reagent cards designed for the ID and antimicrobial susceptibility testing of bacteria… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Missing desiccant. |
| Initiation date | Jan 23, 2018 |
| Report date | Aug 29, 2018 |
| Termination date | Jul 13, 2021 |
| City | Hazelwood |
| State | MO |
| Country | United States |
| FEI number | 1950204 |
At a glance
- 1–9 Products in this recall
- 10–99 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: