Device recall
Z-0272-04: Edwards Lifesciences Vantex Central Venous Catheter Kit with Oligon, Ref/model…
FDA device recall · Class III · Edwards Lifesciences Corporation of Puerto Rico
Key facts
| Recall number (Z-number) | Z-0272-04 |
|---|---|
| Recall event | 27515 |
| Product | Edwards Lifesciences Vantex Central Venous Catheter Kit with Oligon, Ref/model #: 3K20C1827, Rx only, Edwards Lifesciences LLC, Irvine, CA 96214-5686 USA |
| Product code | FOZ |
| Recalling firm | Edwards Lifesciences Corporation of Puerto Rico |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Feb 9, 2004 |
| 510(k) numbers | K992532 |
| FEI number | 2648045 |
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