Device recall
Z-0115-04: CONFIRM c-KIT, Antibody (rabbit polyclonal), Catalog number 790-2939
FDA device recall · Class III · Ventana Medical Systems Inc
Key facts
| Recall number (Z-number) | Z-0115-04 |
|---|---|
| Recall event | 26070 |
| Product | CONFIRM c-KIT, Antibody (rabbit polyclonal), Catalog number 790-2939 |
| Product code | NKF |
| Recalling firm | Ventana Medical Systems Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Mar 30, 2004 |
| FEI number | 1000125183 |
At a glance
- None 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