Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1–5 of 5 recalls
There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits.…
There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits.…
There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits.…
There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits.…
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 potentia…