Device recall
Z-0849-03: Nutriline with Peelable Sheath 2 Fr. is a 2 Fr. peripherally inserted catheter…
FDA device recall · Class II · Vygon Corporation
Key facts
| Recall number (Z-number) | Z-0849-03 |
|---|---|
| Recall event | 26213 |
| Product | Nutriline with Peelable Sheath 2 Fr. is a 2 Fr. peripherally inserted catheter (PIC). Included with this catheter is a 2 Fr. insertion sheath. Product is packaged in tyvek sealed plastic tray. Sterilization occurs via EtO in Germany. |
| Product code | DQO |
| Recalling firm | Vygon Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 3, 2006 |
| 510(k) numbers | K954112 |
| 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