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# Vyaire Recalls Exercise Test Component
- URL: https://www.fdaweb.com/vyaire-recalls-exercise-test-component/
- Published: 2024-05-09T12:00:00.000Z
- Updated: 2026-09-14T14:30:32.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5156948

Vyaire Medical has recalled (Class 1) its Vyaire Twin Tube sample line 240 cm, Model Number V-707327, which is used in the company’s Vyntus CPX cardiopulmonary exercise test device. The Twin Tube line is connected to the adapter for the digital volume transducer that provides an exact determination of ventilation, according to a [recall notice](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=206744&ref=fdaweb.com). It says there is a potential for the Twin Tube’s nozzle to separate during patient use. All lots prior to 6/2023 or with a serial number before # 04I00122 are potentially affected, it adds.