Baxter recalls Blue Ventil: single-patient use circuit for oxygen desaturation or lung injury risk in home care. Affected units have Product Code M07937. Contact for remedy.
Urgent Medical Device Correction for the Volara system single-patient use circuit due to the potential that patients or caregivers may be unaware of a possible decrease in oxygen levels (oxygen desaturation), or potential lung tissue injury from overexpansion (barotrauma) when the Volara device is used in the home care environment. This correction is providing the home caregiver specific instructions for use.
Baxter is recalling Blue Ventilator Adapter Module units (Product Code M07937) because they may cause low oxygen levels or lung injury during home use. This is a serious risk for patients and caregivers using the device at home.
The adapter may cause patients to become oxygen desaturated (low oxygen levels) or suffer lung tissue injury from overexpansion during home use. This happens because caregivers might not notice when oxygen levels drop or the device overexpands the lungs.
Home caregivers using Baxter Volara Respiratory Therapy systems with the recalled Blue Ventilator Adapter Module (Product Code M07937) are at risk. Patients with respiratory conditions are most vulnerable.
Check for Product Code M07937 on the Blue Ventilator Adapter Module. The item is an accessory for Baxter Volara Respiratory Therapy systems sold for home care.
Immediately stop using the Blue Ventilator Adapter Module if it has Product Code M07937.
Yes, the recall applies to home care environments as specified in the hazard description.
The recall states that continued use could cause oxygen desaturation or lung injury, so stopping use is critical.
Look for Product Code M07937 on the Blue Ventilator Adapter Module, which is an accessory for Baxter Volara Respiratory Therapy systems.
We’ve drafted a message you can send Baxter Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1637-2026 — Baxter Healthcare Baxter Healthcare Hello, I own a Baxter Healthcare that is covered by recall Z-1637-2026 from Baxter Healthcare. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
