Device recall
Z-2598-2018: BD FACS Universal Loader (Optional) to the BD FACSLyric Clinical System, Model…
FDA device recall · Class III · Becton, Dickinson and Company, BD Biosciences
Key facts
| Recall number (Z-number) | Z-2598-2018 |
|---|---|
| Recall event | 80388 |
| Product | BD FACS Universal Loader (Optional) to the BD FACSLyric Clinical System, Model 662879 (Universal Loader), Rx Only. The firm name on the label is Becton, Dickinson and Company, BD Biosciences, San Jose, CA. The Loader offers various settings to resuspend and mix samples. It can draw from 12 x 75-mm… |
| Product code | OYE |
| Recalling firm | Becton, Dickinson and Company, BD Biosciences |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 13, 2018 |
| 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