Medline recalls specific convenience kits due to risk of butyrate tubing cracking, making products unusable for medical applications. Affected kits include INPATIENT CENTRAL LN DRSG KIT DYNDC3525 and others.
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 used in hospitals because the liquid adhesive they contain may crack during use, rendering the kits unusable. This could affect medical procedures requiring safe application of catheters.
The kits contain a recalled batch of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing can crack during actuation, which means the product might become unusable for applying catheters.
Healthcare workers using Medline convenience kits in hospitals are most at risk. Patients receiving catheter treatments may be affected if the kits are used improperly.
Check for the model numbers DYNDC3525, DT13191A, CDS982047S, or DYNJ62889C on the kits. The kits were sold with specific lot numbers from 2023.
Identify the model number on the kit to see if it matches DYNDC3525, DT13191A, CDS982047S, or DYNJ62889C.
The kits contain a recalled batch of Ferndale Laboratories MASTISOL Liquid Adhesive that may cause butyrate tubing to crack during use.
Check for the model numbers DYNDC3525, DT13191A, CDS982047S, or DYNJ62889C on the kit. Affected kits were sold with specific lot numbers from 2023.
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-2419-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2419-2026 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.
