Device recall
Z-0995-04: LuMend brand percutaneous catheter.35'' R in plastic sealed bag, sterilized…
FDA device recall · Class II · Lumend Inc
Key facts
| Recall number (Z-number) | Z-0995-04 |
|---|---|
| Recall event | 29212 |
| Product | LuMend brand percutaneous catheter .35'' R in plastic sealed bag, sterilized with ethylene oxide gas. |
| Product code | DQY |
| Recalling firm | Lumend Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 26, 2004 |
| 510(k) numbers | K032298 |
| FEI number | 3002912012 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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