HIGH

Medline Recalls Medical Kits Over Open Seal Hazard

Medline Industries, LP recalled 168 medical convenience kits on December 24, 2025. The kits may contain BD ChloraPrep Triple Swabsticks with open seals. This recall affects products distributed nationwide in the U.S.

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 MERCY CIRCUMCISION TRAY, Kit SKU CIT6135B. It includes BD ChloraPrep Triple Swabsticks. The UDI/DI number is 10653160990666 and Lot Number is 25EBC648.

The Hazard

The hazard arises from the open seal on the packaging of the applicators. This can potentially compromise sterility, leading to increased infection risk.

What to Do

Stop using the recalled kits immediately. Contact Medline Industries or your healthcare provider for further instructions on returning the product.

Contact Information

For more information, visit the FDA recall page at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=Z-1336-2026 or contact Medline Industries directly.

Key Facts

  • Recall date: December 24, 2025
  • Report date: February 18, 2026
  • Quantity recalled: 168 units
  • Open seal may compromise sterility

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 Classification

Product Details

Model Numbers
UDI/DI 10653160990666
Lot Number 25EBC648
Affected States
ALL
Report Date
February 18, 2026
Recall Status
ACTIVE

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