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Smiths Medical ASD Inc. recalls Pneupac paraPAC plus 310 ventilator kit with PEEP and CPAP, REF P310NXX
Recalled September 18, 2024 · FDA recall Z-2974-2024 · Smiths Medical ASD
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. · FDA Class I
Units
10,240 units
Sold at
Worldwide
Description
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.
Product
Pneupac paraPAC plus 310 ventilator kit with PEEP and CPAP, REF P310NXX
Manufacturer(s)
Smiths Medical ASD Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →