Medline recalls specific dialysis kits due to silicone seal issues that could block blood flow or cause leaks. Affected kits include Centurion Central Line Insertion Tray and DIALYSIS BUNDLE with NO CATHETTER. Stop using if you have these kits.
Affected lots may exhibit issues with the silicone seal on Tego Connectors included in kits. Issues include silicone seal doming and silicone seal tearing. These issues may result in an occluded fluid path identified by the inability of the user to inject or withdraw blood product with a syringe. Damaged seals may also result in delay in therapy or fluid leakage, interruption in therapy, exposure to biological contaminants or air infused into the body.
Medline is recalling certain dialysis maintenance kits because the silicone seals on Tego Connectors can dome or tear, potentially blocking blood flow or causing leaks. This could lead to interrupted therapy, fluid leakage, or exposure to contaminants.
The silicone seals in the Tego Connectors may dome or tear, which can block the fluid path needed for blood injection or withdrawal. This could cause therapy interruptions, leaks, or exposure to biological contaminants.
People using dialysis treatments with the recalled kits are most at risk. These kits are used by individuals requiring regular hemodialysis therapy.
Check for the kit lot numbers listed in the recall: 2024121390, 2025033190, 2024051490, 2025021290, 2025051390, 2025091090, and others as detailed in the product list. The kits include Centurion Central Line Insertion Tray, DIALYSIS BUNDLE with NO CATHETTER, and other Medline dialysis components.
Look for the specific lot numbers listed in the recall: 2024121390, 2025033190, 2024051490, 2025021290, 2025051390, 2025091090, and others as detailed in the product list.
No, the recall does not require immediate stop use. However, if you have the affected lot numbers, you should check the kit for seal issues and contact Medline for guidance.
The affected lot numbers include 2024121390, 2025033190, 2024051490, 2025021290, 2025051390, 2025091090, and others as listed in the product description.
The recall states that affected kits may have silicone seal doming or tearing, which could prevent blood injection or withdrawal with a syringe. Check if you can no longer inject or withdraw blood with a syringe.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1465-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1465-2026 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.
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.
