Getinge Servo-i Ventilator Recall: Short Nebulizer Connector May Cause Installation Issues
Getinge recalls Servo-i Ventilators with specific serial numbers due to a potentially shorter nebulizer connector that may cause difficulty installing the Aeroneb Nebulizer module. Affected units can be identified by serial numbers listed in the recall notice.
Lower-risk recall
A potentially shorter than specified nebulizer connector may result in difficulty in installing the Aeroneb Nebulizer module to the Servo-i device successfully.
Contact the company
What happened, in plain English
Getinge is recalling certain Servo-i Ventilators that may have a nebulizer connector shorter than specified. This could make it hard to attach the Aeroneb Nebulizer module properly, potentially affecting patient care. If you own one of these units, check the serial numbers listed in the recall notice. Read more at govinfonow.com/recall/64265-getinge-servo-i-ventilator-recall-short-nebulizer-connector-may-cause.
Source Summary by GovInfoNow · govinfonow.com/recall/64265-getinge-servo-i-ventilator-recall-short-nebulizer-connector-may-cause · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0092-2021
Cite this page
“Getinge Servo-i Ventilator Recall: Short Nebulizer Connector May Cause Installation Issues.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/64265-getinge-servo-i-ventilator-recall-short-nebulizer-connector-may-cause. Based on FDA recall #Z-0092-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0092-2021%22&limit=1).
Why it’s dangerous
The nebulizer connector might be shorter than required, making it difficult to securely attach the Aeroneb Nebulizer module. This could lead to improper function of the ventilator, but the risk is not severe enough to cause serious injury in normal use.
Who’s affected
Healthcare providers using the Servo-i Ventilator for critical or general care, particularly those with the specific serial numbers listed in the recall notice. Patients using these ventilators are at minimal risk if the issue is resolved correctly.
How to tell if you have this one
Check the serial numbers on your Servo-i Ventilator. The affected units have serial numbers starting with 95160 through 97582 (and other numbers listed in the recall notice).
- Brand
Getinge- Category
Medical device
What to do — step by step
Check Serial Numbers
Identify if your ventilator has a serial number listed in the recall notice (e.g., 95160, 95283, etc.).
Where it went and when
Where it was distributed
Distributed in 15 states, and outside the U.S.
FDA distribution: “Domestic distribution to AZ CA GA IL MN MO NC NJ NY RI SC TX VA WI WV Foreign distributed to Bosnia and Herzegovina, Czech Republic, France, Germany, India, Indonesia, Iraq, Italy, Kenya, Republic of Korea, Lebanon, Libyan Arab Jamahiriya,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arizona, California, Georgia, Illinois, Minnesota, Missouri, New Jersey, New York, North Carolina, Rhode Island, South Carolina, Texas, Virginia, West Virginia, Wisconsin.
Recall timeline
FDA published this recall 34 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
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-0092-2021 (September 17, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0092-2021 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 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.