Device recall
Z-2700-2014: Vapotherm Precision Flow,Disposable Patient Circuit PF-E-DPC-High. For use with…
FDA device recall · Class II · Vapotherm, Inc.
Key facts
| Recall number (Z-number) | Z-2700-2014 |
|---|---|
| Recall event | 69116 |
| Product | Vapotherm Precision Flow,Disposable Patient Circuit PF-E-DPC-High. For use with the Precision Flow system Precision Flow" is intended for use to add warm moisture to breathing gases from an external source for administration to a neonate/infant, pediatric and adult patients in the hospital… |
| Product code | BTT |
| Recalling firm | Vapotherm, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 2, 2015 |
| 510(k) numbers | K072845 |
| FEI number | 3012971441 |
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