HIGH

Medline Recalls Blood Culture Kits Due to Open Seal Hazard

Medline Industries, LP recalled 4,300 blood culture kits on December 24, 2025. The recall affects kits containing BD ChloraPrep Triple Swabsticks with packaging that may exhibit an open seal. This defect poses a high risk to patient safety.

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 Blood Culture Kit NS, SKU DYNDH2088. It includes BD ChloraPrep Triple Swabsticks. The kits were distributed nationwide in the United States.

The Hazard

The open seal on the swabstick packaging may compromise sterility. This defect increases the risk of infection in patients.

Reported Incidents

No specific incidents or injuries have been reported as of the recall date. The risk of infection remains a serious concern.

What to Do

Stop using the recalled kits immediately. Patients and healthcare providers should contact Medline Industries for further instructions and possible return options.

Contact Information

For inquiries, call Medline Industries, LP at 1-800-633-5463 or visit the FDA recall page at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=Z-1333-2026.

Key Facts

  • Recall date: December 24, 2025
  • Classification: Class II
  • Quantity recalled: 4,300 kits
  • Risk level: High
  • Packaging defect may lead to infection

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Safety Assessment

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

Product Classification

Product Details

Model Numbers
UDI/DI 10198459230363
Lot Numbers: 25EBU508
25EBE330
Affected States
ALL
Report Date
February 18, 2026
Recall Status
ACTIVE

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