Device recall
Z-2722-2015: Transonic Flow Probe, 6 mm, Catalog Number HQC6FMV -- Product Usage: to measure…
FDA device recall · Class II · Transonic Systems Inc
Key facts
| Recall number (Z-number) | Z-2722-2015 |
|---|---|
| Recall event | 71907 |
| Product | Transonic Flow Probe, 6 mm, Catalog Number HQC6FMV -- Product Usage: to measure flow intra-operatively. |
| Product code | DPW |
| Recalling firm | Transonic Systems Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 18, 2016 |
| 510(k) numbers | K872048 |
| FEI number | 1319030 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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