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.

Smiths Medical ASD Inc. Medical Device Recall: Pneupac paraPAC plus 300 ventilator kit, REF P300NXX | SafeCheck