Vyaire recalls TwinTube sample lines with model V-707327 due to potential nozzle separation during patient use. Affected units sold before June 2023 or with serial numbers before 04I00122.
Potential of the nozzle separating during patient use.
Vyaire is recalling TwinTube sample lines used in medical breath analysis devices because the nozzle might separate during patient use. This could lead to inaccurate test results or discomfort for patients.
The nozzle may separate during patient use, potentially causing inaccurate breath test results or discomfort. This does not pose a direct injury risk but could affect medical study accuracy.
Patients using the TwinTube sample line 240cm with Vyaire's Vyntus CPX device are most at risk. The recall affects units sold before June 2023 or with specific serial numbers.
Check for model number V-707327 on the TwinTube sample line. Units sold before June 2023 or with serial numbers starting with 04I00122 are affected.
Look for model number V-707327 and serial numbers before 04I00122 or units sold before June 2023.
No, the TwinTube sample line is sold outside the US only.
The nozzle may separate during patient use, potentially causing inaccurate test results or discomfort, but not serious injury.
Check for model number V-707327 and serial numbers before 04I00122 or units sold before June 2023.
We’ve drafted a message you can send Vyaire to request your refund or repair — edit it as you like.
Subject: Recall Z-1730-2024 — Vyaire Vyaire Hello, I own a Vyaire that is covered by recall Z-1730-2024 from Vyaire. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
