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. The issue has been associated with improper locking of the nebulizer cup after adding medication during user setup.
Reason for recall: 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. The issue has been associated with improper locking of the nebulizer cup after adding medication during user setup. Distribution: Worldwide distribution - US Nationwide and the country of Canada. Quantity: 13881 units Lot/code info: UDI: 10887761981499; Lot Numbers: All lot numbers distributed beginning on 4/28/2025
10887761981499
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.