Getinge recalls ventilators with model 6882000 (serials 10558-24017) due to stability issues. These devices may tip over when stationary, risking injury during use.
Device does not meet regulatory requirements of stability while stationary, which requires mechanical equipment, other than fixed mechanical equipment, that is intended to be used on the floor or on a table shall be permanently marked with a clearly legible warning of this risk
Getinge is recalling ventilators that could tip over when left stationary, potentially causing injury. This affects specific models sold between 2012 and 2024. Users should check their serial numbers to see if they are affected.
The ventilator may tip over when not secured to a stable surface, which could cause injury to the user or patient. This happens because the device does not meet regulatory stability requirements for equipment intended to be used on floors or tables.
Healthcare professionals and patients using the Servo-air Ventilator System for respiratory support are most at risk. Affected units have specific serial numbers listed in the recall notice.
Check for the model number 6882000 on the device or its cart. Affected units have serial numbers starting with 10558 and ending with 24017, as listed in the recall notice.
Ensure the ventilator is securely anchored to a stable surface before use to prevent tipping.
Compare your device's serial number to the list provided in the recall notice to confirm if it is affected.
Model 6882000 (equipped with 6881999 mobile cart) with serial numbers starting from 10558 to 24017.
Check for the model number 6882000 and verify your serial number against the list of affected numbers (10558-24017) provided in the recall notice.
No, but you should ensure it is securely anchored to prevent tipping. The recall does not require immediate discontinuation.
We’ve drafted a message you can send Getinge to request your refund or repair — edit it as you like.
Subject: Recall Z-1568-2022 — Getinge Getinge Hello, I own a Getinge that is covered by recall Z-1568-2022 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.
