HIGH

Medline Medical Kits Recalled Due to Adhesive Hazard

Medline Industries recalled 1,928 medical procedure convenience kits on December 12, 2025, due to a risk of crack in the adhesive tubing. The kits contain MASTISOL liquid adhesive, leading to safety concerns. Healthcare providers and patients should stop using the kits immediately and follow the recall instructions.

Quick Facts at a Glance

Recall Date
December 12, 2025
Hazard Level
HIGH
Brand
Medline Industries, LP
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

Hazard Information

Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Medline Industries, LP or your healthcare provider for instructions. Notification method: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

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About This Product

Medline medical procedure convenience kits are used in various healthcare settings for procedures that require sterile supplies. They include vital items necessary for patient care and treatment.

Why This Is Dangerous

The kits contain MASTISOL liquid adhesive, which can cause the butyrate tubing to crack during use, leading to potential safety hazards for patients and healthcare providers.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

The recall affects healthcare providers and patients relying on these kits for medical procedures. Users must stop using the kits immediately, which may disrupt care and require alternative supplies.

Practical Guidance

How to identify if yours is affected

  1. Check the SKU on the kit packaging: DT22880 or DYNDC3283A.
  2. Verify the lot numbers: 25KMJ441 for SKU DT22880 or 25KMH515 for SKU DYNDC3283A.
  3. If the SKU matches, the kit is affected by the recall.

Where to find product info

The SKU and lot numbers are typically found on the product packaging or label.

What timeline to expect

Expect a refund or resolution within 4-6 weeks after returning the product.

If the manufacturer is unresponsive

  • Document all communication attempts with Medline.
  • Consider reaching out to the FDA for further assistance.

How to prevent similar issues

  • Look for kits with well-reviewed adhesive alternatives.
  • Check for recent recalls before purchase.
  • Use products from reputable manufacturers with a strong safety record.

Documentation advice

Keep records of your purchase, any correspondence with Medline, and any medical documentation related to the use of the kit.

Product Details

The recall involves two kits: INPATIENT CTRL LN DRG CHG (SKU DT22880) and ADULT CVC DRSG CHG W/ADHESIVE (SKU DYNDC3283A). These kits were distributed nationwide in the United States.

Key Facts

  • 1,928 kits recalled
  • Manufactured with MASTISOL liquid adhesive
  • Stop using product immediately
  • Contact Medline for instructions
  • Distributed nationwide
View Original Recall on FDA - Medical Devices

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Safety Guide

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Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
7/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product TypeMedical Procedure Convenience Kits
Sold At
Multiple Retailers

Product Details

Model Numbers
Medline Kit SKU DT22880: UDI/DI 10653160995470 (EA) 40653160995471 (CS)
Lot Number 25KMJ441
Medline Kit SKU DYNDC3283A: UDI/DI 10198459313240 (EA) 40198459313241 (CS)
Lot Number 25KMH515.
Affected States
ALL
Report Date
February 4, 2026
Recall Status
ACTIVE

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