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Medline Recalls Nerve Block Tray Kits Over Cracked Tubing Risk

Medline Industries recalled medical procedure convenience kits labeled as Nerve Block Tray 2 on December 12, 2025. The recall affects kits containing MASTISOL liquid adhesive due to complaints of cracked butyrate tubing during vial actuation. Healthcare providers and patients should stop using these kits immediately.

Official notice
Medline Industries, LPHealth & Personal CareMedical DevicesUDI/DI 10198459565861 (EA) 40198459565862 (CS)Lot number 25KMD285

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
UDI/DI 10198459565861 (EA) 40198459565862 (CS), Lot number 25KMD285
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 Nerve Block Tray 2 is a medical procedure convenience kit used by healthcare providers for nerve block procedures. These kits are designed to include necessary tools and adhesives for effective medical applications.

Why This Is Dangerous

The hazard arises from the MASTISOL liquid adhesive within the kit, which can crack its butyrate tubing when the vials are actuated. This can lead to chemical exposure, posing health risks.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

The recall affects healthcare providers and patients, requiring immediate cessation of use and potential disruptions in medical procedures.

Practical Guidance

How to identify if yours is affected

  1. Check the SKU on the product: DYNJRA2713.
  2. Verify if the lot number is 25KMD285.
  3. Look for any signs of damage or cracking in the tubing.

Where to find product info

The SKU and lot number can typically be found on the packaging of the kit or the product itself.

What timeline to expect

Expect a refund or replacement processing timeline of approximately 4-6 weeks.

If the manufacturer is unresponsive

  • Contact Medline Industries again using different communication methods.
  • Document all interactions and maintain records of your requests.

How to prevent similar issues

  • Look for products with robust safety certifications.
  • Choose alternative products from reputable manufacturers that have clear safety records.
  • Check for recalls before purchasing medical devices.

Documentation advice

Keep a copy of all correspondence regarding the recall, any receipts, and photos of the product for your records.

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Product Details

The recalled product is the Nerve Block Tray 2, Kit SKU DYNJRA2713. It was distributed nationwide in the U.S. No specific price was mentioned.

Key Facts

  • Recalled product: Nerve Block Tray 2, SKU DYNJRA2713
  • Recall date: December 12, 2025
  • Hazard: Cracked butyrate tubing
  • Action: Stop using and follow recall instructions

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
UDI/DI 10198459565861 (EA) 40198459565862 (CS)
Lot number 25KMD285
Affected States
ALL
Report Date
February 4, 2026
Recall Status
ACTIVE

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