Maquet recalls Servo-n Ventilator System model 6694800 due to potential inaccurate patient circuit compliance measurements during tests, which could affect patient safety.
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.
Maquet is recalling its Servo-n Ventilator System model 6694800 because incorrect pre-use leakage tests combined with an improper humidifier can lead to inaccurate patient circuit compliance measurements. This risk could impact patient safety during ventilator testing.
The ventilator may give incorrect readings about how well the patient's airway works during tests if the pre-use leakage test is done incorrectly or the wrong humidifier is used. This could lead to improper adjustments in the ventilator settings.
Healthcare providers using the Servo-n Ventilator System model 6694800 are likely affected. Patients on ventilators using this model face the lowest risk due to the specific testing conditions required.
Check for the model number 6694800 on the ventilator. The product was sold with all software versions and has a UDI-DI code starting with 07325710001110.
Look for the model number 6694800 on the ventilator or its documentation.
This recall applies to the Servo-n Ventilator System model 6694800. If your ventilator has this model number, it is affected.
The recall does not specify a remedy, so no action is required beyond checking the model number.
Check for the model number 6694800 on the ventilator or its documentation. The product was sold with all software versions and has a UDI-DI code starting with 07325710001110.
We’ve drafted a message you can send Maquet to request your refund or repair — edit it as you like.
Subject: Recall Z-2014-2025 — Maquet Maquet Hello, I own a Maquet that is covered by recall Z-2014-2025 from Maquet. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
