Medline recalls specific convenience kits due to risk of butyrate tubing cracking, making products unusable for central line dressing changes.
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 certain convenience kits for central line dressing changes because the liquid adhesive used in some lots can cause butyrate tubing to crack during use, rendering the kits unusable. This affects healthcare workers who use these kits for patient care.
The kits contain a recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. During use, butyrate tubing may crack, which can make the product unusable for applying dressings to central lines.
Healthcare workers using the recalled Medline convenience kits for central line dressing changes are most at risk. Patients receiving care with these kits could be affected if the kits become unusable.
Check for the product model numbers EBSI1705A, EBSI1057A, EBSI1498, EBSI1585, EBSI1621, or EBSI1837. The recalled lots have specific UDI-DI numbers and production dates listed in the recall notice.
Identify the model number on the kit to see if it matches EBSI1705A, EBSI1057A, EBSI1498, EBSI1585, EBSI1621, or EBSI1837.
Reach out to Medline directly for assistance with the recall process if you have the recalled model.
The recall is due to butyrate tubing cracking during use, which can make the kits unusable for central line dressing changes.
Check the model number and contact Medline for guidance on next steps.
Yes, cracked tubing can render the kits unusable for applying dressings, which could affect patient care.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2438-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2438-2026 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.
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