Maquet Critical Care AB recalls
Every recall we track for Maquet Critical Care AB — 5 in all, from 2025–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Maquet Critical Care AB peaked in 2025 (3); 5 since 2017.
All FDA recall records for Maquet Critical Care AB since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 3 | 0 | 3 |
| 2026 (to date) | 0 | 1 | 0 | 1 | 2 |
What to do if you have a recalled Maquet Critical Care AB product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Maquet Critical Care AB recalls
3 shown- UnratedMedical device
Maquet Critical Care AB recalls GETINGE Y SENSOR Module, SERVO-U, SERVO-N, Model Number 6693662; part of the SERVO-U/-N continuous ventilator system,
Getinge recalls SERVO-U/N ventilator sensor modules (model 6693662) due to untested electrical and functional safety during production. Affected units have specific serial numbers. Consumers should contact Getinge for details.
GetingeJun 30, 2026 - Use cautionMedical device
Maquet Critical Care AB recalls Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 6677300 Flow-i C40 6677400 Flow-i C20 6888520 Flow-i C30 6888530
Maquet recalls Flow-i C20, C30, and C40 anesthesia machines with specific serial numbers due to risk of insufficient anesthesia delivery during surgery, potentially causing patient awareness.
MaquetJun 24, 2026 - Lower riskMedical device
Maquet Critical Care AB recalls Servo-u Ventilator System. Model Number: 6688600.
Maquet recalls Servo-u Ventilator System model 6688600 due to potential inaccurate patient circuit compliance measurements during tests. Affected units may require correction to ensure safe ventilation.
MaquetMay 30, 2025
Maquet Critical Care AB recall questions
How many recalls has Maquet Critical Care AB had?
5 recalls from Maquet Critical Care AB are on record with U.S. safety agencies, from 2025–2026.
What is the most recent Maquet Critical Care AB recall?
Maquet Critical Care AB recalls GETINGE Y SENSOR Module, SERVO-U, SERVO-N, Model Number 6693662; part of the SERVO-U/-N continuous ventilator system,, dated Jun 30, 2026. Every Maquet Critical Care AB recall is listed on this page, newest first.
What should I do if I have a recalled Maquet Critical Care AB product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Maquet Critical Care AB recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.