HIGH

Medline Recalls Medical Kits Over Hazardous Packaging Seal

Medline Industries, LP recalled 120 medical convenience kits on December 24, 2025. The kits contain BD ChloraPrep Triple Swabsticks with potentially 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 recall includes Medline medical convenience kits packaged as ANESTHESIA ARTLINE PACK, Kit SKU DYNJ47387B. The affected model numbers include UDI/DI 10193489217070 and Lot Number 25EBJ414.

The Hazard

An open seal on the packaging of the applicators may lead to contamination. This poses a risk during medical procedures, possibly leading to infection.

Reported Incidents

There have been no reported injuries or incidents linked to this recall at this time. However, due to the nature of the product, the potential for harm exists.

What to Do

Stop using the recalled medical kits immediately. Contact Medline Industries, LP or your healthcare provider for further instructions on returning the products.

Contact Information

For more information, visit the FDA website at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=Z-1326-2026 or contact Medline Industries, LP directly.

Key Facts

  • Recall date: December 24, 2025
  • Total kits recalled: 120
  • Affected model numbers: UDI/DI 10193489217070, Lot Number 25EBJ414
  • No injuries reported at this time

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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 10193489217070
Lot Number 25EBJ414
Affected States
ALL
Report Date
February 18, 2026
Recall Status
ACTIVE

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