Medline convenience kit recall: Butyrate tubing may crack

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Recalling firmMedline Industries, LP3 Lakes Dr · Northfield, IL 60093-2753

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Medline is recalling convenience kits that contain Fernd: Laboratories MASTISOL Liquid Adhesive. The adhesive's butyrate tubing can crack during use, making the product unusable for dressing changes.

Why it’s dangerous

The kits contain Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation, which can render the product unusable for application. This could lead to improper dressing changes.

Who’s affected

Users of Medline convenience kits with the specific model number DYNDC3359 are affected. Healthcare professionals and patients using these kits for dressing changes are at risk.

How to tell if you have this one

Check for the model number DYNDC3359 on the kit. The kits were sold with lot numbers 25KBK310 or 25LBN341.

Brand
Medline
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Kit Model
Look for the model number DYNDC3359 on the kit.

✎ GovInfoNow

Questions people ask

Why is this kit being recalled?

The kits contain Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation, rendering the product unusable for dressing changes.

How can I tell if I have the recalled kit?

Check for the model number DYNDC3359 and lot numbers 25KBK310 or 25LBN341.

What should I do if I have the recalled kit?

The recall record does not specify a remedy or action steps.

Take action

Contact Medline

We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-2426-2026 — Medline Medline

Hello,

I own a Medline that is covered by recall Z-2426-2026 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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Where this comes from

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.

Official source: FDA Recall #Z-2426-2026 (April 27, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2426-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Medline Industries, LP recalls Medline convenience kit: KIT: DRESSING CHANGE PED DYNDC3359

Lower-risk recall