Medline recalls two convenience kits due to risk of butyrate tubing cracking, which can make the product unusable for dressing changes. Affected kits have specific lot numbers from October 2025.
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 two convenience kits that contain a recalled batch of Ferndale Laboratories MASTISOL Liquid Adhesive. The issue could cause butyrate tubing to crack during use, making the product unusable for dressing changes.
The kits contain a recalled batch of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation, which can render the product unusable for applying dressings.
Healthcare workers using Medline convenience kits for port dressing changes are most at risk. Patients using these kits may also be affected if they have specific medical conditions.
Check for the product names: DRIVELINE MANAGEMENT KIT EBSI1688 or PORT DRESSING CHANGE KIT EBSI1328A. Look for lot numbers 2025102890 (EBSI1688) or 2025103090 (EBSI1328A).
Look for lot numbers 2025102890 on EBSI1688 kits or 2025103090 on EBSI1328A kits to confirm if affected.
The kits contain a recalled batch of Ferndale Laboratories MASTISOL Liquid Adhesive that may cause butyrate tubing to crack during use, making the product unusable for dressing changes.
Check for the product names: DRIVELINE MANAGEMENT KIT EBSI1688 or PORT DRESSING CHANGE KIT EBSI1328A with lot numbers 2025102890 or 2025103090.
The recall record does not specify a remedy, so 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-2440-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2440-2026 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.
