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FDAMay 31, 2024device

Pneupac paraPAC plus 310 ventilator kit with PEEP and CPAP, REF P310NXX

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Ongoing

Brands named

smiths medical asdsmithssmiths medical

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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