FDA recall record

Maquet Critical Care AB Servo-u MR Ventilator System recall — FDA Z-2015-2025

Potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to combination of incorrect pre-use leakage…

Class Iclassification
Z-2015-2025official record ID
Jul 9, 2025report date

Recall record at a glance

Official recordZ-2015-2025
CategoryMedical Device Recalls
ClassificationClass I
FDA record statusOngoing
Recalling firmMaquet Critical Care AB
Report dateJul 9, 2025
Recall initiation dateMay 30, 2025
Quantity129 units
LocationSolna, Sweden

Official product description

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

Why the product was 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.

Distribution information

US Nationwide distribution and Puerto Rico. No international distribution.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.