Class I

Medical Device Recall: Pneupac paraPAC plus 310 ventilator kit with PEEP and CPAP, REF P310NXX

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

10,240 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2974-2024

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.