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Medline Circumcision Kits Recalled Over Adhesive Hazard

Medline Industries, LP recalled 1,928 circumcision procedure kits on December 12, 2025. The kits contain MASTISOL liquid adhesive, which may crack during use. Healthcare providers and patients must stop using these kits immediately.

Official notice
Medline Industries, LPHealth & Personal CareMedical DevicesMedline Kit SKU DYNJ16826O: UDI/DI 10195327412067 (EA) 40195327412068 (CS)Lot Number 25LMA655Lot Number 25KMC911.

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
December 12, 2025
Status
ACTIVE
Severity
8/10

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

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Medline Industries, LP
Product type
Medical Procedure Convenience Kits
Model numbers
Medline Kit SKU DYNJ16826O: UDI/DI 10195327412067 (EA) 40195327412068 (CS), Lot Number 25LMA655, Lot Number 25KMC911.
Sold at
Multiple Retailers
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    December 12, 2025

  2. Reported by FDA DEVICE

    February 4, 2026

  3. RecallRadar source check

    February 11, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

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

About This Product

The Medline circumcision kit is designed for surgical procedures involving male circumcision. Healthcare providers use these kits for their convenience and sterile components.

Why This Is Dangerous

The hazard arises from the MASTISOL liquid adhesive, which can crack the butyrate tubing during use, potentially leading to contamination and adverse outcomes.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers must stop using these kits to avoid health risks associated with the adhesive failure. The inconvenience of returning the product and seeking alternatives may also affect healthcare providers.

Practical Guidance

How to identify if yours is affected

  1. Locate the SKU DYNJ16826O on the packaging.
  2. Check the lot numbers: 25LMA655 or 25KMC911.
  3. If your kit matches these identifiers, it is recalled.

Where to find product info

The SKU and lot numbers can be found on the external packaging of the kit or in the product documentation.

What timeline to expect

Expect a refund processing time of approximately 4-6 weeks after returning the product.

If the manufacturer is unresponsive

  • Contact customer service again and document your communication.
  • Reach out to regulatory bodies like the CPSC if the company does not respond.

How to prevent similar issues

  • Always check for product recalls before using medical devices.
  • Look for safety certifications when purchasing medical supplies.
  • Be aware of recent recalls in the healthcare industry.

Documentation advice

Keep all correspondence with the manufacturer, including emails and notes from phone calls. Document any issues with the product, including photos if necessary.

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Product Details

The recalled product is labeled as CIRCUMCISION PACK, Kit SKU DYNJ16826O. The affected UDI/DI numbers are 10195327412067 for each kit and 40195327412068 for cases. Lot numbers include 25LMA655 and 25KMC911.

Key Facts

  • Recalled 1,928 circumcision kits
  • Manufactured by Medline Industries, LP
  • Hazard due to MASTISOL liquid adhesive
  • Stop using the product immediately

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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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 DYNJ16826O: UDI/DI 10195327412067 (EA) 40195327412068 (CS)
Lot Number 25LMA655
Lot Number 25KMC911.
Affected States
ALL
Report Date
February 4, 2026
Recall Status
ACTIVE

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