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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.

Official notice
Medline Industries, LPHealth & Personal CareMedical DevicesUDI/DI 10193489918113Lot Number 25EBD613

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
December 24, 2025
Status
ACTIVE
Severity
7/10

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

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 Convenience Kit
Model numbers
UDI/DI 10193489918113, Lot Number 25EBD613
Sold at
Multiple Retailers
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    December 24, 2025

  2. Reported by FDA DEVICE

    February 18, 2026

  3. RecallRadar source check

    February 25, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

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

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.

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.

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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

  • 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

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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

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