medical MODERATE Updated 2026-08-26

Maquet Critical Care AB recalls GETINGE Y SENSOR Module, SERVO-U, SERVO-N, Model Number 6693

See all recalls from Maquet Critical Care AB →

Recalled Product

GETINGE Y SENSOR Module, SERVO-U, SERVO-N, Model Number 6693662; part of the SERVO-U/-N continuous ventilator system, for facility use. Maquet Critical Care AB, is a subsidiary of Getinge.

Share this recall: Facebook X / Twitter WhatsApp Email

Hazard / Issue

The module did not undergo electrical safety tests and functional tests during production.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: DUI/DI 07325710000304, Serial/Lot Numbers: 21049, 21088, 21089, 21093, 21100, 21103 21108, 21114, 21115.

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

Search Amazon for GETINGE Y SENSOR Module, →

If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.

View official government recall

Related medical Recalls

SDI Limited recalls Dentsply Sirona Capsule Mixer Model No. 5546068

2026-08-26 · Potential for electrical discharge from unit when unplugged.

Arrowhead DE LLC recalls Arrow-LOK Implant, REF: 21-253519, 21-253522, 21-253525,

2026-08-26 · Implant did not undergo required gamma radiation dose audit. A potential reduction in sterility assurance could lead to patient infection.

Tobii Dynavox Llc recalls TD Navio Maxi Speech Generating Device Model/Catalog Number

2026-08-26 · Under certain conditions, the battery mounting tabs may become damaged, allowing the battery to move within the device enclosure, potentially leading to an internal short circuit. This may cause localized heating and gas venting within the device enclosure.

Beckman Coulter Inc. recalls Beckman Coulter DxC 500i Clinical Analyzer Modules using sof

2026-08-26 · a software defect in which the Parameter Package (PP) import logic overwrites all predefined calculated test rules, including those previously modified by the user, upon import of a new Parameter Package version. As a result, usercustomized calculated test rules revert silently to their default expressions, potentially generating erroneous patient test results without an explicit error notification. The issue affects instruments running software version 1.5 or lower and only occurs when a new Parameter Package is imported to a system that already has an existing Parameter Package onboard; new installations are not affected.