Device recall
Z-0132-2011: PD Access Vascular Access Device. Escalon Vascular Access, Inc., 2440 South…
FDA device recall · Class II · Escalon Medical Corp
Key facts
| Recall number (Z-number) | Z-0132-2011 |
|---|---|
| Recall event | 56610 |
| Product | PD Access Vascular Access Device. Escalon Vascular Access, Inc., 2440 South 179th Street, New Berlin, WI 53146: Model 78050 18 Gauge GA Doppler Guided Bare Needle Assembly, 2 3/4 in Length, 0.038 in guidewire, Sterile EO, PD Access Vascular Access Device. Model 78060 Extended 18 Gauge Doppler Guided… |
| Product code | DPW |
| Recalling firm | Escalon Medical Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 28, 2013 |
| 510(k) numbers | K903625 |
| FEI number | 2183477 |
At a glance
- 1–9 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