Medline recalls specific CVC insertion kits due to risk of butyrate tubing cracking, making products unusable. Affected kits include ECVC6805B, ECVC8055A, and others with certain lot numbers.
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Medline is recalling specific central venous catheter (CVC) insertion kits because the butyrate tubing in some kits may crack during use, rendering them unusable. This could lead to failed medical procedures if the kits are used without proper functionality.
The kits contain a recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. When the butyrate tubing is actuated (pulled or pushed), it may crack, making the product unusable for catheter insertion.
Healthcare professionals using the recalled Medline CVC kits are most at risk. Patients receiving care with these kits could face complications if the tubing cracks during insertion.
Check for the model numbers ECVC6805B, ECVC8055A, ECVC6915A, or ECVC6985B with lot numbers 2025120890, 2025112690, 2025102790, or 2025103190.
Look for lot numbers 2025120890, 2025112690, 2025102790, or 2025103190 on the product packaging.
The kits contain a recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive that may cause butyrate tubing to crack during use, making the product unusable.
Check the lot number on the packaging. If it matches the recalled lots (2025120890, 2025112690, 2025102790, or 2025103190), stop using it and contact Medline for instructions.
The recall record does not specify a remedy, so affected users should contact Medline directly for guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2439-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2439-2026 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.
