Medline recalls intubation tray kits (model MNS10395) due to potential weak seals on breather pouches that could lead to contamination during procedures.
There is a potential for open/weak seals on purchased breather pouches used for packaging of select sterile convenience kits.
Medline is recalling intubation tray kits (model MNS1039: MNS10395) because the breather pouches used to package them might have weak seals. This could lead to contamination during medical procedures if the pouches are compromised.
The breather pouches that package the sterile convenience kits may have open or weak seals. If the pouches are compromised during use, they could lead to contamination of the medical equipment.
Healthcare professionals using Medline intubation tray kits (model MNS10395) are affected. Those in settings where these kits are used for procedures are most at risk.
Check for the model number MNS10395 on the kit. The kits were sold with lot number 24KBI045 and were distributed in 2024.
Look for the model number MNS10395 on the intubation tray kit.
Reach out to Medline for guidance on next steps if you have the recalled kit.
The recall is due to potential open or weak seals on breather pouches used to package the sterile convenience kits, which could lead to contamination during medical procedures.
Check for the model number MNS10395 on the intubation tray kit. The kits were sold with lot number 24KBI045 and distributed in 2024.
Contact Medline directly for guidance on next steps if you have the recalled kit.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1586-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1586-2025 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.