Device recall
Z-2826-2018: The Tri-Flo Subglottic Suction System
FDA device recall · Class I · Vyaire Medical
Key facts
| Recall number (Z-number) | Z-2826-2018 |
|---|---|
| Recall event | 80508 |
| Product | The Tri-Flo Subglottic Suction System |
| Product code | BSY |
| Recalling firm | Vyaire Medical |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jul 28, 2020 |
| FEI number | 2050001 |
At a glance
- None 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