Lower riskMedical device recall · FDA · Published May 30, 2025
Maquet Servo-u Ventilator Model 6688600: Inaccurate Circuit Compliance Risk
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.
Take action
Contact the company
📍Recalling firmMaquet Critical Care ABRontgenvagen 2 · Solna, Sweden
“Maquet Servo-u Ventilator Model 6688600: Inaccurate Circuit Compliance Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/52168-maquet-servo-u-ventilator-model-6688600-inaccurate-circuit-compliance-risk. Based on FDA recall #Z-2013-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2013-2025%22&limit=1).
Maquet Critical Care AB voluntarily recalled the Servo-u Ventilator System model 6688600 due to potential inaccurate patient circuit compliance measurements, according to the FDA on May 30, 2025. The recall affects 874 units distributed nationwide and in Puerto Rico.
How to tell if you have it
Brand: Maquet
Product: Servo-u Ventilator System
Model Number: 6688600
UDI-DI: 07325710001042
Quantity: 874 units
The hazard
The hazard involves potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to a combination of incorrect pre-use leakage test and use of an incorrect active humidifier, according to the FDA.
Context
GovInfoNow's records show Maquet Critical Care AB has two other recalls on record since June 24, 2026. Other recent recalls of similar products include Ventec V+Pro Ventilator Recall (March 25, 2026), Maquet Bubble Sensor Recall (January 9, 2026), and Laborie Solar GI System Recall (May 21, 2026).
How to tell if you have this one
Check for the model number 6688600 on the ventilator. The product was sold with UDI-DI: 07325710001042 and all software versions.
Brand
Maquet
Category
Medical device
FDA recall event · 3 products
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class I
Status
Ongoing
Distribution
US Nationwide distribution and Puerto Rico. No international distribution.
Recall number
Product, codes & lots
Quantity
Z-2013-2025
Servo-u Ventilator System. Model Number: 6688600.; Model Number: 6688600. UDI-DI: 07325710001042. All software versions.
874 units
Z-2014-2025
Servo-n Ventilator System. Model Number: 6694800.; Model Number: 6694800. UDI-DI: 07325710001110. All software versions.
7,688 units
Z-2015-2025
Servo-u MR Ventilator System. Model Number: 6888800.; Model Number: 6888800. UDI-DI: 07325710010518. All software versions.
129 units
Based on the official FDA remedy
What to do — step by step
Check for Model Number
Look for the model number 6688600 on the ventilator or its packaging.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “US Nationwide distribution and Puerto Rico. No international distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 40 days after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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.
Official source: FDA Recall #Z-2013-2025 (May 30, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2013-2025 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.