Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Anesthesia gas-machine - Product Usage: intended for use in administering Recalled by Getinge Group Logistics America, LLC Due to Maquet Critical Care AB received complaints where the...
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
Anesthesia gas-machine - Product Usage: intended for use in administering anesthesia while controlling the entire ventilation of patients with no ability to breathe, as well as in supporting patients with limited ability to breathe.
Quantity: 144 units
Why Was This Recalled?
Maquet Critical Care AB received complaints where the FiCO2 value was not zero or as close to zero as expected and/or experienced System Check Out failures when docking the absorber to the Flow i Anesthesia machine.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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