HIGH

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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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.

The Hazard

The packaging of the BD ChloraPrep Triple Swabsticks may exhibit an open seal, which can compromise sterility. This defect poses a high risk of infection or other complications.

Reported Incidents

There are no reported incidents or injuries associated with the recall at this time. Consumers are advised to be vigilant and report any adverse effects.

What to Do

Stop using the recalled Suture Removal Trays immediately. Follow the recall instructions provided by Medline. Contact Medline Industries, LP or your healthcare provider for further guidance.

Contact Information

For more information, visit the Medline website or contact their customer service. The recall details can also be found on the FDA website.

Key Facts

  • Recall date: December 24, 2025
  • Quantity recalled: 2,448 kits
  • Affected packaging may compromise sterility
  • No reported injuries or incidents
  • Contact Medline for further instructions

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Safety Assessment

Risk LevelHIGH
Severity Score
7/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
UDI/DI 10195327379308
Lot Number 25EBO576
Affected States
ALL
Report Date
February 18, 2026
Recall Status
ACTIVE

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