Device recall
Z-0928-03: iVIEW DAB Detecion Kit. Catalog Number 760-091
FDA device recall · Class III · Ventana Medical Systems Inc
Key facts
| Recall number (Z-number) | Z-0928-03 |
|---|---|
| Recall event | 26321 |
| Product | iVIEW DAB Detecion Kit. Catalog Number 760-091 |
| Product code | KTO |
| Recalling firm | Ventana Medical Systems Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 3, 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