Medline recalls convenience kits containing Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during use, rendering kits unusable. Affected kits have specific model numbers and UDI codes.
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 surgical convenience kits because they contain a batch of Ferndale Laboratories MASTISOL Liquid Adhesive that may crack during use. This could make the kits unusable for applying medical products.
The recalled kits contain Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing in these kits may crack during actuation, which can render the product unusable for application. This could lead to improper medical procedures if the kits are used.
Healthcare professionals using Medline convenience kits for surgical procedures are most at risk. Patients receiving these kits during surgery may be affected if the kits are used without proper functionality.
Check for model numbers listed in the recall notice, such as DYNJ64161C, DYNJ47103D, DYNJ67197G, DYNJ85197A, DYNJT4007, and other specific UDI codes. The kits were sold with specific lot numbers and dates.
Identify the model number on the kit, such as DYNJ64161C, DYNJ47103D, or other listed codes.
Reach out to Medline directly for assistance with the recall and to confirm if your kit is affected.
The kits contain a batch of Ferndale Laboratories MASTISOL Liquid Adhesive that may crack during use, rendering the product unusable.
Check the model number on the kit against the list of affected models provided in the recall notice.
Contact Medline directly to confirm if your kit is affected and to get further instructions.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2441-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2441-2026 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.
