Medline recalls chest tube insertion trays that may contain non-sterile product if breather pouch seals are opened. Affected units include specific lot numbers and model CHT1165.
It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.
Medline is recalling chest tube insertion trays that could lead to using non-sterile products if the breather pouch seal is opened. This poses a risk during medical procedures where sterile conditions are critical.
The breather pouch seal may open or become unsealed, allowing non-sterile product to be used during medical procedures. This could lead to infections or complications in sterile environments.
Healthcare professionals using Medline chest tube insertion trays with lot number 24ABB506 are most at risk. Patients undergoing procedures with these trays could face infection risks.
Check for lot number 24ABB506 on the tray packaging. The product model is CHT116: Chest Tube Insertion Tray ADUL.
Inspect the breather pouch for any signs of being opened or unsealed.
The product may contain non-sterile product if the breather pouch seal is opened, so it is not safe to use without checking the seal.
If the pouch seal is open, do not use the product and contact Medline for guidance.
Look for lot number 24ABB506 on the tray packaging. The product model is CHT1165: Chest Tube Insertion Tray ADUL.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0167-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0167-2025 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.