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

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Model Number: 6888800. UDI-DI: 07325710010518. All software versions.
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Maquet Critical Care AB
Reason for Recall:
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.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

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

Product Codes/Lot Numbers:

Model Number: 6888800. UDI-DI: 07325710010518. All software versions.

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2015-2025

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Class I - Dangerous

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.

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Class I - Dangerous

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.

May 30, 2025 Patient Monitors Nationwide View Details →