Device recall
Z-0813-06: TII0002 Implant Tube, Implant Tube, Intralumenal(HDR), 10CM Drawdown 130CM Body…
FDA device recall · Class II · Alpha Omega Services Inc
Key facts
| Recall number (Z-number) | Z-0813-06 |
|---|---|
| Recall event | 34969 |
| Product | TII0002 Implant Tube, Implant Tube, Intralumenal(HDR), 10CM Drawdown 130CM Body, Sealed End, Cable Insert & Gold Seed, Disposable |
| Product code | JAQ |
| Recalling firm | Alpha Omega Services Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 30, 2006 |
| FEI number | 2022694 |
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