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
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