Medline recalls anesthesia circuit kits with cracks in 120" expandable tubing that may leak anesthetics, risking hypoxia and serious injury. Affected kits include specific model numbers and lots.
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 120-inch expandable tubing. These cracks can cause leaks of anesthetic agents, leading to hypoxia, hypoventilation, or inadequate anesthesia delivery, which may cause serious injury or death during surgery.
Cracks in the 120-inch expandable tubing can cause leaks of anesthetic agents. This may lead to hypoxia (low oxygen levels), hypoventilation (inadequate breathing), or insufficient delivery of anesthetic, potentially causing serious injury or death during surgery. Volatile anesthetics may also escape into the operating room environment.
Healthcare professionals using these anesthesia circuit kits during surgery are most at risk. Patients undergoing procedures with these kits could experience serious complications.
Check for model numbers like DYNJAA10591, DYNJAA6555G, or DYNJAA10817. These kits were sold with specific lot numbers (e.g., 25EBU353) between certain dates.
Immediately stop using the recalled anesthesia circuit kits as they can leak anesthetics, risking serious injury or death during surgery.
Cracks in the 120-inch expandable tubing can cause leaks of anesthetic agents, leading to hypoxia, hypoventilation, or inadequate delivery of anesthetic, which may cause serious injury or death.
Affected models include DYNJAA10591, DYNJAA6555G, DYNJAA10817, and others listed in the recall notice with specific lot numbers.
Check the model number on your kit (e.g., DYNJAA10591) and lot number (e.g., 25EBU353) against the list provided in the recall notice.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0442-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-0442-2026 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.
