Device recall
Z-0242-04: VAMP Direct Draw, Model VMP700 Needleless cannula for sampling blood.
FDA device recall · Class II · Edwards Lifesciences AG
Key facts
| Recall number (Z-number) | Z-0242-04 |
|---|---|
| Recall event | 27871 |
| Product | VAMP Direct Draw, Model VMP700 Needleless cannula for sampling blood. |
| Product code | KRA |
| Recalling firm | Edwards Lifesciences AG |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 30, 2004 |
| FEI number | 3003081151 |
At a glance
- None 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