Medline recalls anesthesia circuit kits with cracks in tubing that may leak, risking hypoxia and serious injury during surgery. Affected kits include OPEN HEART SUPPLEMENT DYNJ909116D and others.
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 and cause low oxygen levels or inadequate anesthesia delivery during surgery. This poses a serious risk to patients under anesthesia.
Cracks in the 120-inch expandable tubing can cause leaks of anesthesia. This may lead to low oxygen levels, insufficient anesthesia delivery, or dangerous levels of volatile anesthetics escaping into the operating room.
Healthcare professionals using anesthesia circuit kits for surgeries. Patients undergoing surgery are at risk if the kit leaks.
Check for kits labeled with model numbers DYNJ909116D, DYNJ909124F, or UDI-DI numbers 40198459055356/40198459130619. These were sold in lots 25FBM604, 25GBP604, 25FBB831, or 25GBI833.
Immediately stop using any recalled anesthesia circuit kits with cracks in the tubing as they can cause leaks leading to serious injury or death.
The recalled kits include model numbers DYNJ909116D, DYNJ909124F, and UDI-DI numbers 40198459055356/40198459130619.
Multiple complaints reported cracks in the 120-inch expandable tubing, which can leak anesthesia and cause hypoxia or serious injury during surgery.
Check for model numbers DYNJ909116D, DYNJ909124F, or UDI-DI numbers 40198459055356/40198459130619, sold in lots 25FBM604, 25GBP604, 25FBB831, or 25GBI833.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0444-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-0444-2026 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.
