Medline recalls specific convenience kits containing Ferndale Laboratories MASTISOL Liquid Adhesive with butyrate tubing that may crack during use, rendering kits unusable.
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 several convenience kits that contain a recalled batch of Ferndale Laboratories MASTISOL Liquid Adhesive. The butyrate tubing in these kits may crack during use, making the products unusable for application.
The kits contain Ferndale Laboratories MASTISOL Liquid Adhesive with butyrate tubing that may crack during actuation. This cracking can render the product unusable for application, but it does not cause injury or pose a direct risk to users.
Healthcare professionals using Medline convenience kits with the specific model numbers listed in the recall. The risk is low as the issue only affects the tubing during use and does not cause immediate injury.
Check for the model numbers listed in the recall, such as DYNJ905869G, DYNJ68484B, DYNJ58305, and others. The kits were sold with specific UDI-DI numbers and lots (e.g., Lot 25JBX559).
Identify if your kit matches the model numbers listed in the recall, such as DYNJ905869G or DYNJ68484B.
Reach out to Medline directly for assistance with the recall or to confirm if your kit is affected.
The kits contain Ferndale Laboratories MASTISOL Liquid Adhesive with butyrate tubing that may crack during use, rendering the product unusable.
Check for the model numbers listed in the recall, such as DYNJ905869G, DYNJ68484B, DYNJ58305, and others, along with the specific UDI-DI numbers and lots.
Contact Medline directly to confirm if your kit is affected and for guidance on next steps.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2424-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2424-2026 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.
