Device recall
Z-1628-2010: CELL-DYN 1700, list numbers 03H5301 and 03H53-03, manufactured by Abbott…
FDA device recall · Class II · Abbott Laboratories
Key facts
| Recall number (Z-number) | Z-1628-2010 |
|---|---|
| Recall event | 53212 |
| Product | CELL-DYN 1700, list numbers 03H5301 and 03H53-03, manufactured by Abbott Hematology, Santa Clara, CA |
| Product code | gkz |
| Recalling firm | Abbott Laboratories |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 3, 2010 |
| 510(k) numbers | K870233 |
| FEI number | 2919069 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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