FDAMay 31, 2024device

paraPAC plus 310 ventilator kit with internal PEEP and CPAP, Item Number P310N

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

The hazard

Smiths Medical became aware of an issue related to a potential for the patient outlet connector to loosen/detach from the paraPAC Plus P300 and P310 ventilators impacting the active ventilation function.

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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