Medline recalls specific convenience kits containing Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during use, rendering kits unusable for medical applications.
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 specific batch of Ferndale Laboratories MASTISOL Liquid Adhesive. The adhesive's butyrate tubing can crack during use, making the kits unusable for medical applications.
The kits contain a recalled batch of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing in this adhesive can crack during actuation, which means the product may become unusable for medical applications. This does not pose an immediate risk of injury to users.
Healthcare professionals using Medline convenience kits with the specific model numbers and lots listed in the recall notice. Patients receiving care using these kits are at low risk since the kits are not in direct use during normal medical procedures.
Check if your Medline convenience kit has model numbers: LOOP PACK DYNJ61460C, OPEN HEART CDS840150Y, PACEMAKER DYNJ56297C, PACEMAKER PK DYNJT3454, or other listed models. Look for specific lot numbers like 25KBA098, 25JBW220, etc., as listed in the recall notice.
Identify your Medline convenience kit model from the list provided in the recall notice.
Reach out to Medline directly for assistance with the recall process.
The kits contain a specific batch of Ferndale Laboratories MASTISOL Liquid Adhesive where butyrate tubing may crack during use, rendering the product unusable for medical applications.
Check if your kit has model numbers listed in the recall notice, such as LOOP PACK DYNJ61460C or OPEN HEART CDS840150Y, and specific lot numbers like 25KBA098.
Contact Medline directly for assistance with the recall process.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2418-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2418-2026 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.
