Medline recalls specific robotic surgical tubes due to cracks causing anesthesia leaks that may lead to serious injury or death 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 certain robotic surgical tubes because cracks in the tubing can cause anesthesia leaks. This may lead to serious injury or death during surgery if the leaks cause inadequate anesthetic delivery or hypoxia.
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 delivery of anesthetic agents, potentially causing serious injury or death during surgery.
Surgical teams using the recalled Medline robotic surgical tubes are at risk. Patients undergoing surgery with these tubes could face serious injury or death due to anesthesia leaks.
Check for the model numbers DYNJ909119G, DYNJ909127F, or DYNJ909129D on the tubes. The specific serial numbers and lots are listed in the recall notice for verification.
Immediately stop using the recalled surgical tubes as they can cause serious injury or death during surgery.
DYNJ909119G (Robotic Gastric Lap Sleeve-LF), DYNJ909127F (Cysto), and DYNJ909129D (General Laparoscopy-LF).
Cracks in the 120-inch expandable tubing can cause anesthesia leaks, leading to hypoxia, hypoventilation, and inadequate anesthetic delivery, which may cause serious injury or death.
Look for the model numbers DYNJ909119G, DYNJ909127F, or DYNJ909129D on the tubes, and verify the serial numbers and lots listed 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-0446-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-0446-2026 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.
