Device recall
Z-2421-2010: CELL-DYN Sapphire Probe Detector PCB Assembly (also called the Aspiration Bottom…
FDA device recall · Class II · Abbott Laboratories
Key facts
| Recall number (Z-number) | Z-2421-2010 |
|---|---|
| Recall event | 56422 |
| Product | CELL-DYN Sapphire Probe Detector PCB Assembly (also called the Aspiration Bottom Sensor) used on the Cell-Dyn Sapphire Hematology Analyzer, Manufactured by Abbott Laboratories, Santa Clara, CA |
| Product code | GKZ |
| Recalling firm | Abbott Laboratories |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 17, 2011 |
| 510(k) numbers | K051215 |
| 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