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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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.

The Hazard

The MASTISOL liquid adhesive in these kits may cause butyrate tubing to crack during use. This defect poses a risk of exposure to potentially harmful substances.

Reported Incidents

No specific incidents have been reported yet. The recall is based on complaints regarding the cracking of tubing.

What to Do

Stop using the recalled kits immediately. Contact Medline Industries for further instructions on returning the product.

Contact Information

For more information, visit Medline's website or call their customer service line. The recall notice is available at the FDA's enforcement report.

Key Facts

  • 60 units recalled
  • SKU P903933B affected
  • Lot Number 25KMA871
  • Stop using immediately
  • Follow manufacturer instructions

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

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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