HIGH

Medline Recalls IV Administration Sets Due to Valve Malfunction

Medline Industries recalled 12 IV administration kits on November 26, 2025. The kits may contain defective check valve components that can become stuck. Patients and healthcare providers should stop using these devices immediately.

Quick Facts at a Glance

Recall Date
November 26, 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 contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.

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: Letter

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About This Product

Medline IV Administration Sets are used in healthcare settings to deliver medications and fluids intravenously. These products are essential for patient care in various medical procedures.

Why This Is Dangerous

The malfunction of the check valve components can disrupt the flow of medication, which may lead to serious complications in patient treatment.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Patients relying on these IV administration sets may face significant health risks. Immediate action is required to ensure safety.

Practical Guidance

How to identify if yours is affected

  1. Verify the model numbers: UDI/DI 10884389725092 and 40884389725093.
  2. Check the lot number: 25IBC144.
  3. Review the notification letter received from Medline.

Where to find product info

Model numbers and lot numbers can be found on the packaging or product label of the IV sets.

What timeline to expect

Expect a refund or replacement processing time of about 4-6 weeks after returning the product.

If the manufacturer is unresponsive

  • Document all communication attempts with Medline.
  • Contact the FDA or CPSC for further assistance if needed.

How to prevent similar issues

  • Always check for recalls before using medical devices.
  • Look for safety certifications on medical products.
  • Ensure proper training for healthcare professionals using IV administration sets.

Documentation advice

Keep records of your correspondence regarding the recall, including dates and descriptions of communication.

Product Details

The recall involves Medline kits containing B. Braun IV Administration Sets and Pump Administration Sets, specifically labeled as NEURO ANGIO PACK, Medline kit SKU DYNJ38935. The affected models include UDI/DI 10884389725092 (EA) and 40884389725093 (CS), with lot number 25IBC144.

Key Facts

  • Recall date: November 26, 2025
  • 12 units recalled
  • Affected models include UDI/DI 10884389725092 and 40884389725093
  • Lot number 25IBC144

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 10884389725092 (EA) 40884389725093 (CS)
Lot number 25IBC144
Affected States
ALL
Report Date
January 21, 2026
Recall Status
ACTIVE

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