Device recall
Z-0173-2020: Emerald Diluent Tubing, List number 09H50-01, accompanying CELL-DYN Emerald…
FDA device recall · Class II · Abbott Laboratories
Key facts
| Recall number (Z-number) | Z-0173-2020 |
|---|---|
| Recall event | 83793 |
| Product | Emerald Diluent Tubing, List number 09H50-01, accompanying CELL-DYN Emerald instrument, List number 09H39-01. The firm name on the label is Abbott Laboratories, Abbott Park, IL. |
| Product code | GKZ |
| Recalling firm | Abbott Laboratories |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 7, 2020 |
| 510(k) numbers | K081495 |
| 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