HIGH

Medline Recalls Medical Kits Over Open Seal Hazard

Medline Industries, LP recalled 21,854 medical kits on December 24, 2025, due to potential packaging defects. The recall affects kits containing BD ChloraPrep Triple Swabsticks with compromised seals. Patients and healthcare providers must stop using these kits immediately.

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

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About This Product

Medline Kits are essential medical supplies used in various healthcare settings for procedures requiring sterilization and precision. They are often used in hospitals, clinics, and by healthcare providers to ensure patient safety and hygiene during medical interventions.

Why This Is Dangerous

The defect involves an open seal on the packaging of BD ChloraPrep Triple Swabsticks, which may compromise their sterility. This increases the risk of infection when used on patients.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers should stop using these kits to avoid potential health risks. The recall creates an immediate need for replacements, impacting healthcare providers and patients relying on these products.

Practical Guidance

How to identify if yours is affected

  1. Check the SKU and lot number on your medical kit packaging.
  2. Compare your product details with the recall announcement.
  3. If your product matches any listed SKU or lot number, it is affected.

Where to find product info

The SKU and lot numbers can usually be found on the outer packaging of the medical kits or on the accompanying documentation.

What timeline to expect

Expect a refund processing timeline of 4-6 weeks after returning the recalled product.

If the manufacturer is unresponsive

  • Contact Medline Industries directly via phone or email.
  • Document all communication attempts for your records.
  • Consider reaching out to regulatory authorities if the company does not respond.

How to prevent similar issues

  • Look for seals on packaging to ensure sterility when purchasing medical supplies.
  • Check for FDA recalls before using medical products.
  • Choose reputable brands known for quality assurance.

Documentation advice

Keep a copy of your purchase receipt and any correspondence with Medline regarding the recall.

Product Details

The recall includes various Medline Kits with SKUs DT22010B, DT22790C, DYNDA2966A, DYNDC2208C, DYNDC3107, and others. The affected lots include 25EBC888, 25EBO566, 25EBD964, 25EBN178, and 25EBL624. These kits were distributed nationwide in the United States.

Key Facts

  • Recall date: December 24, 2025
  • Quantity recalled: 21,854 units
  • Hazard classification: Class II
  • Affected kits include multiple SKUs and lot numbers
  • No injuries or deaths reported

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 Details

Model Numbers
1) Kit SKU DT22010B
UDI/DI 10653160351092
Lot number 25EBC888
2) Kit SKU DT22790C
UDI/DI 10653160996965
+13 more
Affected States
ALL
Report Date
February 18, 2026
Recall Status
ACTIVE

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