Vyaire Medical GmbH — Class I medical device recall Z-1730-2024
Ongoing recall by Vyaire Medical, Inc., reported 2024-05-15, distributed nationwide. Potential of the nozzle separating during patient use.
| Recall number | Z-1730-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Vyaire Medical, Inc., Hochberg, N/A, Germany |
| Recall initiated | 2024-04-08 |
| Classified | 2024-05-08 |
| Reported by FDA | 2024-05-15 |
| Distributed | Nationwide (US) |
| Quantity | 649 devices |
| UPC / GTIN / UDI-DI | 14250892903603 |
| Model numbers | V-707327 |
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 for recall
Potential of the nozzle separating during patient use.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1730-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.