Device recall
Z-2254-2013: POWERWAND Safety Introducer with Extended Dwell Catheter; Catalog no. 92006…
FDA device recall · Class II · Access Scientific Inc
Key facts
| Recall number (Z-number) | Z-2254-2013 |
|---|---|
| Recall event | 66223 |
| Product | POWERWAND Safety Introducer with Extended Dwell Catheter; Catalog no. 92006. Used to gain access to the vascular system to sample blood and administer fluids intravenously. |
| Product code | DYB |
| Recalling firm | Access Scientific Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 24, 2013 |
| 510(k) numbers | K111417, K121748, K131300 |
| FEI number | 3009549229 |
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