Device recall
Z-0737-2018: OptiView Amplification Kit (250 Test), Ventana Part Number 860-099, Roche GMMI…
FDA device recall · Class I · Ventana Medical Systems Inc
Key facts
| Recall number (Z-number) | Z-0737-2018 |
|---|---|
| Recall event | 78942 |
| Product | OptiView Amplification Kit (250 Test), Ventana Part Number 860-099, Roche GMMI 06718663001 in vitro diagnostic |
| Product code | NJT |
| Recalling firm | Ventana Medical Systems Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Nov 22, 2021 |
| FEI number | 1000125183 |
At a glance
- None Linked 510(k)s
- 10–99 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