Fabian™ HFO Ventilator
Brand(s)
Summary
Contact the manufacturer if you require additional information.
Affected products
Affected products |
Lot or serial number |
Model or catalog number |
---|---|---|
Fabian™ HFO Ventilator |
All lots. |
112001 |
Issue
Software V5.2.2 changed the criteria for detecting a patient circuit disconnect during HFO ventilation with the intent to reduce the potential for patient safety-related risks.
While ventilating in HFO mode with pressure amplitude (Pamp) > 1.5x mean pressure (Pmean) and with the breathing circuit properly connected, if the breath-by-breath leak monitor exceeds 40%, the ventilator triggers the disconnect alarm. the displayed volume and leak monitors reset to zero and the ventilator reduces the HFOV amplitude as a protection mechanism to prevent lung injury upon reconnection following a true disconnection. If the patient is not disconnected, this results in a small increase in Pmean, and potentially large reduction in amplitude until the alarm is cleared.
The potential health risk for a false disconnect alarm occurring that cannot be resolved is inadequate ventilation due to the oscillation being out of range, resulting in hypoxia, hypercapnia, hypoventilation and/or respiratory arrest.
Recall start date: April 17, 2024
Additional information
Details
Acutronic Medical Systems AG
Fabrik Im Schiffli, Hirzel, Switzerland, 8816
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