Device recall
Z-0935-2012: FloWire Doppler Guide wires. Volcano Corporation, Rancho Cardova, Ca. The…
FDA device recall · Class II · Volcano Corporation
Key facts
| Recall number (Z-number) | Z-0935-2012 |
|---|---|
| Recall event | 60842 |
| Product | FloWire Doppler Guide wires. Volcano Corporation, Rancho Cardova, Ca. The Volcano FloWire Doppler guide wire is a single use guide wire intended for use in all blood vessels including both coronary and peripheral arteries to measure blood flow velocities during diagnostics angiography and/or… |
| Product code | DQX |
| Recalling firm | Volcano Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 1, 2012 |
| 510(k) numbers | K972762 |
| FEI number | 2939520 |
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