Medline recalls convenience kits with potential anesthesia circuit leaks causing hypoxia and serious injury. Affected kits include specific model numbers and lots. Stop using immediately to prevent risks.
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 for robotic surgery that may have cracks in the anesthesia tubing. These cracks can cause leaks leading to serious injury or death during surgery.
Cracks in the 120-inch expandable tubing can cause leaks of anesthesia. This may lead to hypoxia (low oxygen), hypoventilation (inadequate breathing), and insufficient delivery of anesthetic agents, risking serious injury or death.
Surgical teams using Medline's convenience kits for robotic procedures are at risk. Patients undergoing surgery with these kits could face serious injury or death due to anesthesia leaks.
Check for model numbers DYNJ901046M (GYN ROBOTIC) or DYNJ909120D (ROBOTIC PROSTATE) with specific lot numbers listed in the recall notice.
Discard the convenience kit if you have the affected model numbers and lots listed in the recall notice.
DYNJ901046M (GYN ROBOTIC) and DYNJ909120D (ROBOTIC PROSTATE) with specific lot numbers listed in the recall notice.
Multiple complaints of anesthesia circuit leaks due to cracks in the 120-inch expandable tubing.
Leaking anesthesia can cause hypoxia, hypoventilation, and inadequate delivery of anesthetic agents, potentially leading to serious injury or death.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0450-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-0450-2026 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.
