Medline recalls convenience kits with potential anesthesia circuit leaks causing hypoxia and serious injury. Affected kits include specific models and lots. Stop using immediately to prevent risks during surgery.
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 several convenience kits for spine surgery that have cracks in the tubing, which can leak anesthesia and cause serious injury or death. These leaks may lead to inadequate anesthetic delivery or dangerous oxygen levels during surgery.
Cracks in the 120-inch expandable tubing can cause leaks in the anesthesia circuit. This may lead to hypoxia (low oxygen), hypoventilation (inadequate breathing), and insufficient anesthetic delivery, potentially causing serious injury or death during surgery. Volatile anesthetics can also escape into the operating room.
Spine surgery patients and medical staff using the recalled convenience kits. Those with the specific model numbers and lots listed are most at risk.
Check for model numbers: DYNJ901047R, DYNJ902308K, DYNJ909111F, DYNJ909117G, or DYNJ909113F. Look for specific lots: 25FBE036, 25GBV759, 25FBR230, 25GBU693, 25FBO307, 25GBN625, 25FBB321, 25GBU688, 25IBM788.
Discontinue use of the recalled convenience kits to prevent potential leaks during surgery.
The affected models include DYNJ901047R (ORTHO SPINE FUMICH), DYNJ902308K (TOTAL JOINT), DYNJ909111F (DR SALMA'S SPINE), DYNJ909117G (PATTERSON TOTAL JOINT), and DYNJ909113F (KYPHOPLASTY).
Check the model number and lot number on your kit. Affected kits have specific model numbers and lots listed in the recall notice.
The recall does not provide a remedy; affected kits must be stopped from use immediately.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0451-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-0451-2026 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.
