Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Servo-i Ventilator Recalled by Getinge Group Logistics America, LLC Due to A potentially shorter than specified nebulizer connector may...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Getinge Group Logistics America, LLC directly.
Affected Products
Servo-i Ventilator, Part No. 6487800, UDI Code 07325710000823 - Product Usage: intended for general and critical ventilator care, and it can be used for low end to high end intensive care, in different configurations. It supports a variety of breathing modes and can be used for Neonates, Pediatric and Adults.
Quantity: 431 units
Why Was This Recalled?
A potentially shorter than specified nebulizer connector may result in difficulty in installing the Aeroneb Nebulizer module to the Servo-i device successfully.
Where Was This Sold?
This product was distributed to 15 states: AZ, CA, GA, IL, MN, MO, NJ, NY, NC, RI, SC, TX, VA, WV, WI
About Getinge Group Logistics America, LLC
Getinge Group Logistics America, LLC has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report