Device recall
Z-0792-2019: BD FACSLyric 3L 10C with FACSuite Clinical Software v1.1.1, catalog number…
FDA device recall · Class III · Becton, Dickinson and Company, BD Biosciences
Key facts
| Recall number (Z-number) | Z-0792-2019 |
|---|---|
| Recall event | 81915 |
| Product | BD FACSLyric 3L 10C with FACSuite Clinical Software v1.1.1, catalog number 662878 BD FACSLyric is a high-performance flow cytometer designed to support both routine clinical analysis and research for the identification, quantification, and characterization of cells in support of cell analysis. BD… |
| Product code | OYE |
| Recalling firm | Becton, Dickinson and Company, BD Biosciences |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 7, 2021 |
| 510(k) numbers | K170974 |
| FEI number | 2916837 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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