Device recall
Z-1112-04: Cell-Dyn 1000 series platelet analyzer (model numbers 1300, 1400, 1600, 1700…
FDA device recall · Class II · Abbott Laboratories
Key facts
| Recall number (Z-number) | Z-1112-04 |
|---|---|
| Recall event | 29434 |
| Product | Cell-Dyn 1000 series platelet analyzer (model numbers 1300, 1400, 1600, 1700, 1800) |
| Product code | GKL |
| Recalling firm | Abbott Laboratories |
| Recall class | Class II |
| Status | Terminated on August 11, 2004 |
| FEI number | 3016438761 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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