Device recall
Z-0071-2008: NeoMedix Trabectome I/A Console, Model Number 550014, surgical aspirator
FDA device recall · Class II · Neomedix Corp
Key facts
| Recall number (Z-number) | Z-0071-2008 |
|---|---|
| Recall event | 48721 |
| Product | NeoMedix Trabectome I/A Console, Model Number 550014, surgical aspirator |
| Product code | BTA |
| Recalling firm | Neomedix Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 29, 2008 |
| 510(k) numbers | K040239 |
| FEI number | 3003698071 |
At a glance
- 1–9 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