FDAMay 30, 2025device

Servo-u MR Ventilator System. Model Number: 6888800.

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

The hazard

Potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to combination of incorrect pre-use leakage test and use of an incorrect active humidifier.

What to do

FDA enforcement status: Ongoing

Brands named

maquet critical care abmaquetmaquet critical

UPCs

07325710010518

Recall history

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

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →