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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.

Official notice
Medline Industries, LPHealth & Personal CareMedical DevicesUDI/DI 10198459230363Lot Numbers: 25EBU50825EBE330.

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
December 24, 2025
Status
ACTIVE
Severity
8/10

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

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Medline Industries, LP
Product type
Medical Convenience Kits
Model numbers
UDI/DI 10198459230363, Lot Numbers: 25EBU508, 25EBE330.
Sold at
Multiple Retailers
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    December 24, 2025

  2. Reported by FDA DEVICE

    February 18, 2026

  3. RecallRadar source check

    February 25, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

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

About This Product

The Medline Blood Culture Kit is used for collecting samples in medical settings to detect infections. Healthcare providers rely on these kits to ensure sterile procedures when obtaining blood samples.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers who have purchased these kits should stop using them immediately, posing an urgent need for safe alternatives to ensure patient care.

Practical Guidance

How to identify if yours is affected

  1. Locate the SKU DYNDH2088 on the product packaging.
  2. Check the lot numbers 25EBU508 and 25EBE330.
  3. Verify if the seal on the swabsticks is intact.

Where to find product info

The SKU and lot numbers can typically be found on the outer packaging or label of the kit.

What timeline to expect

Expect processing for refunds or replacements to take approximately 4-6 weeks.

If the manufacturer is unresponsive

  • Contact Medline Industries again to follow up on your request.
  • Document all correspondence regarding the recall.

How to prevent similar issues

  • Always check for seal integrity before using medical kits.
  • Look for certifications or quality assurance labels on medical products.
  • Purchase from reputable suppliers to minimize recall risks.

Documentation advice

Keep records of your purchase, including receipts and correspondence related to the recall.

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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.

Key Facts

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

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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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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