HIGH

Medline Medical Kits Recalled Over Tubing Cracking Hazard

Medline Industries recalled 60 medical procedure convenience kits on December 12, 2025. The kits contain MASTISOL liquid adhesive which has a defect causing butyrate tubing to crack. Users must stop using the kits immediately and follow 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

The Medline medical procedure convenience kits are designed for healthcare applications, providing necessary tools for procedures like shaving prior to surgery. Consumers typically purchase these kits for clinical settings where sterile procedures are required.

Why This Is Dangerous

The defect in the MASTISOL liquid adhesive kits is due to the butyrate tubing cracking, which can compromise the integrity of the adhesive and potentially expose users to harmful substances.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers should immediately stop using these kits to avoid potential exposure to unsafe materials. The recall could lead to inconvenience for healthcare providers who rely on these kits.

Practical Guidance

How to identify if yours is affected

  1. Check the SKU on the packaging: P903933B.
  2. Look for the Lot Number: 25KMA871.
  3. Verify if the kit is still in use.

Where to find product info

The SKU and Lot Number can typically be found on the product packaging or included in the user manual.

What timeline to expect

Expect 4-6 weeks for processing any refunds or replacements after contacting Medline.

If the manufacturer is unresponsive

  • Contact Medline customer service again.
  • Document all communications for reference.
  • Consider reaching out to regulatory authorities if unresolved.

How to prevent similar issues

  • Always check recall notices for medical supplies before purchase.
  • Look for alternative brands with strong safety records.
  • Ensure products are certified by regulatory agencies.

Documentation advice

Keep a record of your purchase, including receipts and any correspondence with the manufacturer regarding the recall.

Product Details

The recalled product is the HEAD SHAVE-LATEX SAFE KIT, Kit SKU P903933B. The affected lot number is 25KMA871. These kits were distributed nationwide in the US.

Key Facts

  • 60 units recalled
  • SKU P903933B affected
  • Lot Number 25KMA871
  • Stop using immediately
  • Follow manufacturer instructions
View Original Recall on FDA - Medical Devices

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Safety Guide

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 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 P903933B: UDI/DI 10889942362080 (EA) 40889942362081 (CS)
Lot Number 25KMA871
Affected States
ALL
Report Date
February 4, 2026
Recall Status
ACTIVE

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