Medline recalls specific dialysis dressing kits with silicone seal issues that may cause blood flow problems, delayed therapy, or fluid leakage. Affected kits include EBSI1498, EBSI1107, and others.
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 dressing kits that have silicone seals which may dome or tear. This can cause problems with blood flow during dialysis, leading to delayed treatment, fluid leaks, or exposure to contaminants.
The silicone seals in the Tego Connectors can dome or tear, which may block the fluid path. This prevents proper blood flow during dialysis, potentially causing treatment delays, fluid leaks, or exposure to contaminants.
Healthcare professionals using Medline dialysis dressing kits with specific SKUs and lot numbers are affected. Patients receiving dialysis treatments using these kits are at risk of complications.
Check for kits with model numbers EBSI1498, EBSI1107, EBSI1596, EBSI1781, EBSI1812, DT22630, EBSI1470, or DT22845. Look for specific lot numbers listed in the recall notice.
Review the lot numbers provided in the recall notice to determine if your kit is affected.
Reach out to Medline directly for guidance on whether your kit is affected and what steps to take.
Affected kits include Medline DIALYSIS DRESSING CHANGE SKU EBSI1498, EBSI1107, EBSI1596, EBSI1781, EBSI1812, Centurion DIALYSIS/PHERESUS CVC DRSG CHANGE KIT SKU DT22630, Medline DIALYSIS/PHERESIS DRESSING CHANGE KIT SKU EBSI1470, and Centurion VASCATH DRESSING CHANGE TRAY SKU DT22845.
The recall does not specify a remedy, so contact Medline directly to determine if your kit is affected and what steps to take.
Damaged seals may cause blood flow issues, delayed therapy, fluid leakage, or exposure to contaminants, but the recall does not specify a risk of serious injury.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1467-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1467-2026 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.
