Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
Servo-u MR Ventilator System. Model Number: 6888800. Recalled by Maquet Critical Care AB Due to Potential for inaccurate measurement of the patient circuit...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Maquet Critical Care AB directly.
Affected Products
Servo-u MR Ventilator System. Model Number: 6888800.
Quantity: 129 units
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Maquet Critical Care AB
Maquet Critical Care AB has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report