Medline recalls specific convenience kits due to risk of butyrate tubing cracking, making products unusable for arterial insertion. Affected kits include ADD-A-CATH ARTNC185 and DYNDC3291 models.
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 that contain a recalled batch of Ferndale Laboratories MASTISOL Liquid Adhesive. This adhesive can cause butyrate tubing to crack during use, making the kits unusable for arterial insertion procedures.
The kits contain a specific batch of Ferndale Laboratories MASTISOL Liquid Adhesive that can cause butyrate tubing to crack when activated. This cracking makes the product unusable for applying catheters during arterial insertion procedures.
Healthcare workers using Medline convenience kits for arterial insertion procedures are most at risk. Patients receiving these kits may be affected if the kits are used without the adhesive being functional.
Check for the model numbers ARTNC185 or DYNDC3291 on the kits. The affected kits were sold with specific lot numbers: Lot 25JBU463 for ARTNC185 and Lot 25KBH082 for DYNDC3291.
Identify the model number on the kit (ARTNC185 or DYNDC3291) to determine if it is affected.
The kits contain a recalled batch of Ferndale Laboratories MASTISOL Liquid Adhesive that can cause butyrate tubing to crack during use, making the kits unusable for arterial insertion procedures.
The recall record does not specify a remedy, so no action is required beyond checking if your kit is affected.
Yes, affected kits include ARTNC185 Lot 25JBU463 and DYNDC3291 Lot 25KBH082.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2445-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2445-2026 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.
