HIGHFDA DEVICE

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.

Official notice
Medline Industries, LPHealth & Personal CareMedical DevicesUDI/DI 10884389725092 (EA) 40884389725093 (CS)Lot number 25IBC144

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
November 26, 2025
Status
ACTIVE
Severity
8/10

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

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
IV Administration Set
Model numbers
UDI/DI 10884389725092 (EA) 40884389725093 (CS), Lot number 25IBC144
Sold at
Multiple Retailers
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    November 26, 2025

  2. Reported by FDA DEVICE

    January 21, 2026

  3. RecallRadar source check

    April 13, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

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

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.

Get instant alerts for Health & Personal Care recalls

Be the first to know. Free instant alerts to your inbox.

No spamUnsubscribe anytime

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
  • 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

Get Alerts for Health & Personal Care Recalls

Get instant alerts for recalls that affect you. Free forever.

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

Related Recalls