Device recall
Z-1730-2024: Vyaire Medical GmbH, Vyaire Twin Tube sample line 240 cm, Model Number V-707327…
FDA device recall · Class I · Vyaire Medical, Inc.
Key facts
| Recall number (Z-number) | Z-1730-2024 |
|---|---|
| Recall event | 94256 |
| Product | Vyaire Medical GmbH, Vyaire Twin Tube sample line 240 cm, Model Number V-707327; The TwinTube sample line 240cm is used in the Vyntus CPX. The TwinTube sample line 240cm is connected to the adapter for DVT. Twin Tube Probenschlauch (707004), which is sold outside the US only. Used in breath analysis… |
| Product code | BZC |
| Recalling firm | Vyaire Medical, Inc. |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K150810 |
| FEI number | 1000271197 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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