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.
A potentially shorter than specified nebulizer connector may result in difficulty in installing the Aeroneb Nebulizer module to the Servo-i device successfully.
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.
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.
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.
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).
Identify if your ventilator has a serial number listed in the recall notice (e.g., 95160, 95283, etc.).
The nebulizer connector may be shorter than specified, which could make it difficult to install the Aeroneb Nebulizer module properly.
Check the serial number on your ventilator against the list of affected numbers provided in the recall notice (e.g., 95160, 95283, etc.).
No action is needed if your ventilator's serial number is not listed in the recall notice.
We’ve drafted a message you can send Getinge to request your refund or repair — edit it as you like.
Subject: Recall Z-0092-2021 — Getinge Getinge Hello, I own a Getinge that is covered by recall Z-0092-2021 from Getinge. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
