Maquet Critical Care AB 2025-07-09 Health critical FDA
Health · FDA · Recall #FDA-Z-2013-2025
Servo-u Ventilator System. Model Number: 6688600. Recall
Issued July 9, 2025 · Maquet Critical Care AB
In July 2025, Maquet Critical Care AB recalled the Servo-u Ventilator System. Model Number: 6688600., a critical health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
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.
What you should do
- 1 Stop using Servo-u Ventilator System. Model Number: 6688600. right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Maquet Critical Care AB to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Maquet Critical Care AB
- Category
- Health
- Recall date
- July 9, 2025
- Units affected
- Not reported
- Sold at
- US Nationwide distribution and Puerto Rico. No international distribution.
- Recall number
- FDA-Z-2013-2025
- Made in
- Sweden
- Issuing agency
- FDA
In context
- Maquet Critical Care AB has 1 recall in our database, including 1 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.