HIGH

Medline Recalls Sterile Resection Kits Due to Open Seal Hazard

Medline Industries, LP announced a recall of 216 kits packaged as Sterile Resection Packs on December 24, 2025. The kits contain BD ChloraPrep Triple Swabsticks that may have an open seal. The recall affects healthcare providers and patients nationwide.

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 Sterile Resection Pack, SKU DYNDL1980A. It includes BD ChloraPrep Triple Swabsticks. The kits were distributed in the United States.

The Hazard

The BD ChloraPrep Triple Swabsticks may exhibit an open seal on the packaging, compromising sterility. This defect increases the risk of infection during medical procedures.

Reported Incidents

There are no reported incidents of injury or harm associated with this recall. However, the potential risk of infection is significant.

What to Do

Stop using the Sterile Resection Kits immediately. Follow recall instructions provided by Medline Industries, LP. Contact Medline or your healthcare provider for further guidance.

Contact Information

For more information, contact Medline Industries, LP directly or visit their website. Additional information is available on the FDA recall page.

Key Facts

  • 216 kits recalled
  • Open seal may compromise sterility
  • No reported injuries or incidents
  • Contact Medline for further instructions
  • Nationwide distribution in the US

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product TypeMedical Convenience Kits
Sold At
Multiple Retailers

Product Details

Model Numbers
UDI/DI 10195327379292
Lot Number 25EBJ785
Affected States
ALL
Report Date
February 18, 2026
Recall Status
ACTIVE

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