Device recall
Z-1390-2016: BD-Retic-Count Reticulocyte Reagent System; Hematology: Used for in vitro…
FDA device recall · Class III · Becton, Dickinson and Company, BD Biosciences
Key facts
| Recall number (Z-number) | Z-1390-2016 |
|---|---|
| Recall event | 73597 |
| Product | BD-Retic-Count Reticulocyte Reagent System; Hematology: Used for in vitro diagnostics |
| Product code | GKL |
| Recalling firm | Becton, Dickinson and Company, BD Biosciences |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Dec 2, 2016 |
| 510(k) numbers | K880636 |
| 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