Medline Recalls Suture Removal Trays Due to Seal Failure
Medline Industries, LP recalled 2,448 Suture Removal Trays on December 24, 2025. The recall affects kits containing BD ChloraPrep Triple Swabsticks with potentially open seals. The company urges immediate cessation of use to avoid potential hazards.
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
The Suture Removal Tray is used in medical settings for removing sutures safely and effectively. Consumers purchase these kits for both professional healthcare use and home care.
Why This Is Dangerous
The open seal on the BD ChloraPrep Triple Swabsticks can lead to contamination, compromising patient safety. Users may unknowingly apply a non-sterile product, increasing the risk of infection.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Consumers should stop using these kits immediately to prevent potential health risks. The recall may cause delays in treatment for those relying on these kits.
Practical Guidance
How to identify if yours is affected
Check the SKU DYNDR1277A on the packaging.
Look for Lot Number 25EBO576 on the product.
Verify the UDI/DI 10195327379308 against the recall list.
Where to find product info
You can find the SKU and Lot Number on the outer packaging or the product insert.
What timeline to expect
Expect a refund or replacement process to take approximately 4-6 weeks.
If the manufacturer is unresponsive
Document your communication attempts with Medline.
Contact your healthcare provider for assistance.
File a complaint with the FDA if necessary.
How to prevent similar issues
Examine packaging for integrity before purchase.
Choose products from reputable manufacturers with good safety records.
Stay informed about recalls in the medical product category.
Documentation advice
Keep a record of your purchase, including receipts and any correspondence related to the recall.
Product Details
The recalled product is the Suture Removal Tray, Kit SKU DYNDR1277A, with UDI/DI 10195327379308 and Lot Number 25EBO576. These kits were distributed nationwide in the United States.
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