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

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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.

The Hazard

The recall stems from concerns that the packaging of the applicators may exhibit an open seal. This defect could compromise the sterility of the swabsticks, leading to potential health risks.

Reported Incidents

There have been no reported injuries or incidents related to this recall. The situation remains active with ongoing monitoring.

What to Do

Users should stop using the affected kits immediately. Contact Medline Industries, LP or your healthcare provider for detailed instructions on returning the product.

Contact Information

For further details, call Medline Industries at 1-800-633-5463 or visit their website at www.medline.com.

Key Facts

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

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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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