On January 17, 2026, the FDA announced an urgent recall of certain Medline anesthesia kits due to the potential for serious injury or death. This recall affects anesthesia circuit kits containing 120″ anesthesia tubing, which may be used in medical facilities across the US.
What Changed?
Medline has issued a recall of affected products after receiving multiple complaints of anesthesia circuit leaks during leak testing and patient use. The leaks are caused by cracks in the 120″ expandable tubing, which can lead to compromised ventilation and anesthetic delivery.
Who is Affected?
Medical facilities and healthcare professionals who use Medline anesthesia circuit kits are affected by this recall. Patients who undergo procedures using these kits are also at risk of serious injury or death due to potential ventilation failure or inadequate delivery of inhaled anesthetic agents.
Device Use
An anesthesia breathing circuit is a device intended to administer medical gases to a patient during anesthesia. It provides both an inhalation and exhalation route and may include a connector, adaptor, and Y-piece.
Reason for Recall
The reason for the recall is the potential for cracks and leaks in the anesthesia circuit tubing, which can lead to serious injury or death. As of October 31, Medline has not reported any serious injuries or deaths associated with this issue. However, the FDA has identified 7 events related to the recall issue where oxygen desaturation occurred, resulting in serious injury.
What to Do
Customers in the US with adverse reactions, quality problems, or questions about this recall should contact Medline at 866-359-1704 or recalls@medline.com. Healthcare professionals and consumers may report adverse reactions or quality problems they experienced using these devices to MedWatch: The FDA Safety Information and Adverse Event Reporting Program.
Conclusion
In conclusion, the FDA recall of Medline anesthesia kits is a serious issue that affects medical facilities and healthcare professionals across the US. It is essential to take immediate action to remove affected products from use and to report any adverse reactions or quality problems to Medline or the FDA.
Disclaimer
This information is not intended to be legal advice. Healthcare professionals and medical facilities should consult with their legal counsel to ensure compliance with FDA regulations and guidelines.
For Full Information
For full information about the FDA announcement, see the link below.
https://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/anesthesia-kit-recall-medline-removes-anesthesia-circuits-and-anesthesia-circuit-kits