Medline recalls anesthesia circuit kits with cracks causing leaks that may lead to hypoxia, hypoventilation, or inadequate anesthetic delivery. Stop using immediately to prevent serious injury or death.
Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120" expandable tubing. Cracks and resulting leaks may lead to hypoxia, hypoventilation, and inadequate delivery of inhaled anesthetic agents, which may result in serious injury or death. Volatile anesthetics may also escape into the operating room environment.
Medline is recalling anesthesia circuit kits that have cracks in the tubing, which can leak anesthetic agents. This may cause low oxygen levels, breathing problems, or serious injury or death during surgery.
Cracks in the expandable tubing can cause leaks of anesthetic agents. This may lead to low oxygen levels, breathing difficulties, or inadequate delivery of anesthetic, potentially causing serious injury or death during surgery.
Healthcare professionals using the recalled anesthesia circuit kits for surgeries are most at risk. Patients undergoing anesthesia could face serious complications if the kit leaks.
Look for the model number CIRCUIT,ANES,EXTENDFLEX,120,LF DYNJAA10230 on the kit. The kit was sold with lot numbers 25EBV570 and 25FBT843.
Discard the recalled anesthesia circuit kit to prevent leaks that could cause serious injury or death.
Multiple complaints reported cracks in the 120" expandable tubing causing leaks of anesthetic agents.
Leaks may lead to hypoxia, hypoventilation, inadequate anesthetic delivery, or serious injury or death during surgery.
Check for model number CIRCUIT,ANES,EXTENDFLEX,120,LF DYNJAA10230 with lot numbers 25EBV570 or 25FBT843.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0449-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-0449-2026 from Medline. 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.
