Device recall
Z-2717-2014: CelluTome Epidermal Harvesting System Part number CT-H25 or Part Number CT-H50
FDA device recall · Class II · KCI USA, Inc.
Key facts
| Recall number (Z-number) | Z-2717-2014 |
|---|---|
| Recall event | 68329 |
| Product | CelluTome Epidermal Harvesting System Part number CT-H25 or Part Number CT-H50 |
| Product code | GFD |
| Recalling firm | KCI USA, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 18, 2015 |
| FEI number | 3005178245 |
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