Device recall
Z-0090-06: Premicath 28G PICC Catheter
FDA device recall · Class II · Vygon Corporation
Key facts
| Recall number (Z-number) | Z-0090-06 |
|---|---|
| Recall event | 32997 |
| Product | Premicath 28G PICC Catheter |
| Product code | LJS |
| Recalling firm | Vygon Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 31, 2005 |
| 510(k) numbers | K041468 |
| FEI number | 2245270 |
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