Device recall
Z-0365-06: 6 cm Catheter Reservoir with 10 cm extension
FDA device recall · Class III · Vygon Neuro
Key facts
| Recall number (Z-number) | Z-0365-06 |
|---|---|
| Recall event | 32533 |
| Product | 6 cm Catheter Reservoir with 10 cm extension |
| Product code | HCA |
| Recalling firm | Vygon Neuro |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jan 10, 2006 |
| 510(k) numbers | K853361 |
| FEI number | 2518608 |
At a glance
- 1–9 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