Device recall
Z-0451-2007: Drew Excell 22 Hematology Analyzer, manufactured by Drew Scientific, Inc…
FDA device recall · Class II · Drew Scientific Group PLC
Key facts
| Recall number (Z-number) | Z-0451-2007 |
|---|---|
| Recall event | 36728 |
| Product | Drew Excell 22 Hematology Analyzer, manufactured by Drew Scientific, Inc., Dallas, TX. |
| Product code | GKZ |
| Recalling firm | Drew Scientific Group PLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 10, 2008 |
| 510(k) numbers | K991539 |
| FEI number | 3003071743 |
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