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Anesthesia Kit Recall: Medline Removes Anesthesia Circuits and Anesthesia Circuit Kits 

The FDA is aware that Medline has issued a letter to affected customers recommending certain Anesthesia Circuit Kits and other kits containing Anesthesia Circuits be removed from where they are used or sold. Medline has received multiple complaints of anesthesia circuit leaks during leak testing and patient use due to cracks in the 120” expandable tubing, resulting in potential compromised ventilation and anesthetic delivery.  

This recall involves removing certain devices from where they are used or sold. The FDA has identified this recall as the most serious type. This device may cause serious injury or death if you continue to use it.  

Questions?

Customers in the U.S. with adverse reactions, quality problems, or questions about this recall should contact Medline at 866-359-1704 or recalls@medline.com.