HIGH

Medline Recalls Medical Convenience Kits Over Open Seal Hazard

Medline Industries, LP recalled 1,350 medical convenience kits on December 24, 2025. The recall affects kits containing BD ChloraPrep Triple Swabsticks with potential open seals. Users should cease using these kits immediately and follow manufacturer instructions for return.

Quick Facts at a Glance

Recall Date
December 24, 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 Industries, LP is issuing a recall for specific items and lots of Medline Kits containing BD ChloraPrep Triple Swabsticks which BD determined may exhibit an open seal on the packaging of the applicators.

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

Get instant alerts for Health & Personal Care recalls

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

No spamUnsubscribe anytime

About This Product

The Medline medical convenience kits are used for healthcare procedures requiring sterile swabs. They are commonly utilized in both clinical and home healthcare settings.

Why This Is Dangerous

The open seal on the packaging can expose the swabsticks to contaminants, compromising their sterility and increasing infection risk.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Users face potential health risks if they continue using the affected kits. Immediate cessation of use is necessary to ensure safety.

Practical Guidance

How to identify if yours is affected

  1. Check the SKU DYNDC3109 on the packaging.
  2. Look for the lot number 25EBD613.
  3. Verify if the seal on the applicators is intact.

Where to find product info

Serial numbers and lot information can typically be found on the product packaging or accompanying documentation.

What timeline to expect

Expect a refund process timeline of approximately 4-6 weeks after returning the product.

If the manufacturer is unresponsive

  • Contact Medline Industries directly for follow-up.
  • Document all communication attempts for your records.

How to prevent similar issues

  • Always check the packaging for integrity before use.
  • Purchase medical supplies from reputable sources with clear labeling.
  • Stay informed on recalls through healthcare providers.

Documentation advice

Keep copies of receipts, emails, and any official communication regarding the recall.

Product Details

The recalled product is the Medline medical convenience kit, SKU DYNDC3109. It includes BD ChloraPrep Triple Swabsticks. These kits were distributed nationwide in the U.S.

Key Facts

  • 1,350 kits recalled
  • Open seal on applicator packaging
  • Class II recall
  • Nationwide distribution in the U.S.

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
7/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Details

Model Numbers
UDI/DI 10193489918113
Lot Number 25EBD613
Affected States
ALL
Report Date
February 18, 2026
Recall Status
ACTIVE

Related Recalls

Vehicles & Parts
HIGH

Mazda CX-70 Recall 2025 for Powertrain Control Module Software May Lose Drive Power

Mazda North American Operations is recalling 2024 CX-90 and 2025 CX-70 SUVs sold through Mazda dealers. The PCM and ECM software can illuminate malfunction indicator lights and cause a loss of drive power, increasing crash risk. Owner notification letters were mailed December 19, 2024, and Mazda will reprogram the PCM and ECM at no charge.

Mazda
Loss of
Read more
Vehicles & Parts
HIGH

Nissan Kicks 2025 Certification Label Recall for GVWR/GAWR Errors (PD136, PMA47)

Nissan North America is recalling certain 2025 Nissan Kicks vehicles sold through Nissan dealers nationwide. The certification label may print incorrect GVWR and GAWR values, risking overload. Some SR trims with a 19-inch wheel package may display an incorrect wheel size on the label, and owners should contact their Nissan dealer to arrange replacement labels.

Nissan
An overloaded
Read more