Device recall
Z-2166-2018: The VITEK 2 Anaerobic and Corynebacteria identification card (ANC) is intended…
FDA device recall · Class II · BioMerieux SA
Key facts
| Recall number (Z-number) | Z-2166-2018 |
|---|---|
| Recall event | 80111 |
| Product | The VITEK 2 Anaerobic and Corynebacteria identification card (ANC) is intended for use with the VITEK 2 Systems for the automated identification of most clinically significant anaerobic organisms and Corynebatcerium species. The VITEK 2 ANC identification card is a single-use disposable. A… |
| Product code | JSP |
| Recalling firm | BioMerieux SA |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 23, 2020 |
| FEI number | 1000611339 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database