Device recall
Z-0711-04: AngioDynamics Incorporated 21 Gauge Micro Access Needle, B-Bevel - 4 cm length…
FDA device recall · Class II · Enpath Medical, Inc.
Key facts
| Recall number (Z-number) | Z-0711-04 |
|---|---|
| Recall event | 28419 |
| Product | AngioDynamics Incorporated 21 Gauge Micro Access Needle, B-Bevel - 4 cm length, catalog No. 06506803 |
| Product code | GAA |
| Recalling firm | Enpath Medical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 25, 2006 |
| FEI number | 2183787 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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