Medline recalls anesthesia circuit kits with leaks that could cause oxygen deprivation or death during surgery. Affected kits include BREATHING KIT-LF DYNJ105: 10889942469703 (ea) and 40889942469704 (case).
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 may leak due to cracks in the tubing. This can cause oxygen deprivation or death during surgery. The recall affects specific kits sold with lot numbers 25EBQ445.
Cracks in the 120" expandable tubing can cause leaks of anesthesia. This may lead to oxygen deprivation, inadequate anesthetic delivery, or dangerous levels of volatile anesthetics in the operating room.
Surgical staff and patients using the recalled anesthesia circuit kits. Those with the specific lot numbers 25EBQ445 are most at risk.
Check for the model number DYNJ10550 on the kit. Look for lot number 25EBQ445 on the case or individual units.
Immediately stop using the recalled anesthesia circuit kits with the model DYNJ10550 and lot number 25EBQ445.
The recall is due to cracks in the 120" expandable tubing causing leaks that may lead to oxygen deprivation or death during surgery.
The affected kits include BREATHING KIT-LF DYNJ10550 with lot number 25EBQ445 (case: 40889942469704, unit: 10889942469703).
Check for the model number DYNJ10550 and lot number 25EBQ445 on the kit's packaging or label.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0443-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-0443-2026 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.
