Class I

Medical Device Recall: Pneupac paraPAC plus 300 ventilator kit, REF P300NXX

Smiths Medical ASD Inc. · May 31, 2024

Reason for Recall

There is a potential for inadvertent tidal volume knob movement from the original setting when set at high (1000-1500 mL) and low (70-150 mL) settings.

Distribution

Worldwide

Quantity Affected

2198 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2973-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.