Getinge SERVO-U/N Ventilator Sensor Module Recall: Untested Electrical Safety
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.
Recall notice
The module did not undergo electrical safety tests and functional tests during production.
What happened, in plain English
Getinge is recalling certain SERVO-U and SERVO-N ventilator sensor modules because they were not properly tested for electrical and functional safety during manufacturing. This could lead to electrical issues or malfunctions that might affect patient safety. Read more at govinfonow.com/recall/697972-getinge-servo-u-n-ventilator-sensor-module-recall-untested-electrical.
Source Summary by GovInfoNow · govinfonow.com/recall/697972-getinge-servo-u-n-ventilator-sensor-module-recall-untested-electrical · Updated September 14, 2026 · FDA enforcement record: FDA #Z-2963-2026
Cite this page
“Getinge SERVO-U/N Ventilator Sensor Module Recall: Untested Electrical Safety.” GovInfoNow, updated September 14, 2026. https://govinfonow.com/recall/697972-getinge-servo-u-n-ventilator-sensor-module-recall-untested-electrical. Based on FDA recall #Z-2963-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2963-2026%22&limit=1).
Why it’s dangerous
The sensor modules were not tested for electrical safety and functionality during production. This could result in electrical malfunctions or failures that might impact the ventilator's operation, potentially affecting patient safety.
Who’s affected
Healthcare facilities using the specific model and serial numbers listed in the recall notice are affected. Patients and staff using these ventilators may be at risk if the sensor module fails.
How to tell if you have this one
Check for the model number 6693662 on the sensor module. Affected units have serial numbers: 21049, 21088, 21089, 21093, 21100, 21103, 21108, 21114, 21115.
- Brand
Getinge- Category
Medical device
What to do — step by step
Check Serial Numbers
Verify if your sensor module has the listed serial numbers: 21049, 21088, 21089, 21093, 21100, 21103, 21108, 21114, 21115.
Where it went and when
Where it was distributed
Distributed nationwide; the notice names 4 states.
FDA distribution: “US Nationwide distribution in the states of CA, GA, MN, NY.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: California, Georgia, Minnesota, New York.
Recall timeline
FDA published this recall 57 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #Z-2963-2026 (June 30, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2963-2026 to see it in context.
- Plain-language summary written by qwen3:4b on September 14, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.