Medline recalls convenience kits with cracks in expandable tubing that may cause anesthesia leaks, leading to hypoxia or death during surgery. 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 convenience kits that have cracks in the expandable tubing, which can leak anesthesia and cause serious injury or death during surgery. This recall affects specific model numbers and production lots.
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 improper delivery of anesthetic agents, potentially causing serious injury or death during surgery. Volatile anesthetics can also escape into the operating room.
Healthcare professionals using these kits during surgery are most at risk. The recall applies to specific model numbers and production lots sold to hospitals and surgical centers.
Check for model numbers DYNJ901048N, DYNJ909123F, DYNJ909132F, or DYNJ909308D on the kits. Affected lots include 25FBB311, 25GBC282, 25GBW486, 25GBQ070, 25GBI845, 25IBF708, 25GBT826, and 25IBF707.
Discontinue use of the affected convenience kits to prevent potential anesthesia leaks and serious injury.
Affected models include DYNJ901048N (Ortho Spine St Clair), DYNJ909123F (Urology Minor), DYNJ909132F (Set Up), and DYNJ909308D (Hip Pinning).
Affected lots are 25FBB311, 25GBC282, 25GBW486, 25GBQ070, 25GBI845, 25IBF708, 25GBT826, and 25IBF707.
Check the model number and lot number on the kit. Affected kits have specific model numbers and the listed production lots.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0448-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-0448-2026 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.
