Maquet recalls Servo-u Ventilator System model 6688600 due to potential inaccurate patient circuit compliance measurements during tests. Affected units may require correction to ensure safe ventilation.
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-u Ventilator System model 6688600 because incorrect pre-use leakage tests and humidifier use can cause inaccurate circuit compliance measurements. This could lead to improper ventilation settings if not corrected.
The ventilator may give inaccurate readings of how well the patient's airway works during tests. This happens when the pre-use leakage test is done incorrectly or the wrong humidifier is used. Inaccurate readings could lead to improper ventilation settings.
Healthcare professionals using the Servo-u Ventilator System model 6688600 are most at risk. Patients receiving ventilation support could be affected if the system provides incorrect compliance readings.
Check for the model number 6688600 on the ventilator. The product was sold with UDI-DI: 07325710001042 and all software versions.
Look for the model number 6688600 on the ventilator or its packaging.
This recall applies to Maquet Servo-u Ventilator System model 6688600 with UDI-DI: 07325710001042 and all software versions.
The recall does not specify a remedy, so no action is required beyond checking if you have the model number 6688600.
The recall states potential for inaccurate measurements, but no specific risk of serious injury is mentioned.
We’ve drafted a message you can send Maquet to request your refund or repair — edit it as you like.
Subject: Recall Z-2013-2025 — Maquet Maquet Hello, I own a Maquet that is covered by recall Z-2013-2025 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.
