Device recall
Z-2001-2014: VTI BAYONET DOPPLER, 20MHz DOPPLER PROBE, SLIM, BX 4, REF 108660 The Doppler…
FDA device recall · Class II · Vascular Technology, Inc.
Key facts
| Recall number (Z-number) | Z-2001-2014 |
|---|---|
| Recall event | 68512 |
| Product | VTI BAYONET DOPPLER, 20MHz DOPPLER PROBE, SLIM, BX 4, REF 108660 The Doppler probe is intended for the intraoperative and transcutaneous evaluation of blood flow. |
| Product code | DPW |
| Recalling firm | Vascular Technology, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 11, 2016 |
| 510(k) numbers | K082870 |
| FEI number | 1221072 |
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