Device recall
Z-1711-2009: Laborie Medical Technologies Urodynamic Catheters, Twin Lumen 6 Fr, 40cm For…
FDA device recall · Class III · Laborie Medical Technologies Cor
Key facts
| Recall number (Z-number) | Z-1711-2009 |
|---|---|
| Recall event | 52431 |
| Product | Laborie Medical Technologies Urodynamic Catheters, Twin Lumen 6 Fr , 40cm For Cystometry. Catalog Number: CAT-206. |
| Product code | EXQ |
| Recalling firm | Laborie Medical Technologies Cor |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Aug 20, 2009 |
| FEI number | 3017448360 |
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