Device recall
Z-1438-2017: CELL-DYN Ruby System: List Number: 08H6701; Hematology: The CELL-DYN Ruby System…
FDA device recall · Class II · Abbott Laboratories
Key facts
| Recall number (Z-number) | Z-1438-2017 |
|---|---|
| Recall event | 76481 |
| Product | CELL-DYN Ruby System: List Number: 08H6701; Hematology: The CELL-DYN Ruby System is a multi-parameter automated hematology analyzer designed for in-vitro diagnostic use in clinical laboratories |
| Product code | GKZ |
| Recalling firm | Abbott Laboratories |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 6, 2018 |
| 510(k) numbers | K061667 |
| FEI number | 2919069 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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