Baxter Healthcare Corporation Oscillation Lung Expansion Therapy, positive pressure breathing device

Source: FDA | Recall date: 05/21/2026

Don't want to manually check every recall?

Track your baby products and get automatic recall alerts when something may affect your family.

Start Free Recall Tracking How Tracking Works

Learn more about the baby product recall tracker, automatic email item adding, or recall monitoring plans.

Affected product: Oscillation Lung Expansion Therapy, positive pressure breathing device

Brand: baxter healthcare corporation

Hazard: There have been reports of air and medication leakage f⁠rom the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an oxygen level drop in the patient and ineffective nebulization, which may affect the delivery of the prescribed treatment.

Official identifiers

FDA recall number: Z-2550-2026
FDA event number: 99119

Open FDA Enforcement Record Back to Home Search FDA recall records

Don't want to manually check every recall?

Track your baby products and get automatic recall alerts when something may affect your family.

Start Free Recall Tracking How Tracking Works

Learn more about the baby product recall tracker, automatic email item adding, or recall monitoring plans.