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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About This Product
Medical convenience kits are used in various healthcare settings for procedures requiring sterile swabs. These kits are purchased by healthcare providers to ensure patient safety during medical treatments.
Why This Is Dangerous
An open seal on the packaging of the BD ChloraPrep Triple Swabsticks may compromise sterility, increasing the risk of infection during medical procedures.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
The recall affects the availability of these medical kits, which are essential for maintaining sterility during procedures. Healthcare providers must ensure they have safe alternatives available.
Practical Guidance
How to identify if yours is affected
Check the SKU number on the packaging.
Verify if the kit is labeled as ANESTHESIA ARTLINE PACK, Kit SKU DYNJ47387B.
Look for the affected model numbers: UDI/DI 10193489217070 and Lot Number 25EBJ414.
Where to find product info
The SKU number can typically be found on the outer packaging of the medical kit.
What timeline to expect
Expect refund processing to take 4-6 weeks after returning the product.
If the manufacturer is unresponsive
Document all communication attempts with Medline.
Contact the FDA if the company remains unresponsive.
How to prevent similar issues
Always check for seals and packaging integrity before use.
Purchase from reputable suppliers to ensure product safety.
Stay updated on recalls involving medical devices.
Documentation advice
Keep a record of your purchase, including receipts, and document any correspondence regarding the recall.
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.
Key Facts
Recall date: December 24, 2025
Total kits recalled: 120
Affected model numbers: UDI/DI 10193489217070, Lot Number 25EBJ414
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