FDA Device recall Z-1730-2024
Vyaire Medical GmbH, Vyaire Twin Tube sample line 240 cm, Model Number V-707327
- FDA Device
- Class I
- ongoing
- Published 2024-05-15
On 2024-05-15 the FDA classified a Class I recall of Vyaire Medical GmbH, Vyaire Twin Tube sample line 240 cm, Model Number V-707327 by Vyaire Medical, citing potential of the nozzle separating during patient use.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1730-2024 |
| Classification | Class I |
| Status | ongoing |
| Initiated | 2024-04-08 |
| Published | 2024-05-15 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Vyaire Medical |
| Distribution | US |
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 for metabolic response study.
Reason
Potential of the nozzle separating during patient use.
Identifiers
| code_info | UDI/DI 14250892903603, All lots prior to June 2023 or with a serial number before 04I00122 are potentially affected. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1730-2024%22
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