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Medline Recalls Medical Kits Over Hazardous Packaging Seal

Medline Industries, LP recalled 120 medical convenience kits on December 24, 2025. The kits contain BD ChloraPrep Triple Swabsticks with potentially open seals. This recall affects products distributed nationwide in the U.S.

Official notice
Medline Industries, LPHealth & Personal CareMedical DevicesUDI/DI 10193489217070Lot Number 25EBJ414

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 10193489217070, Lot Number 25EBJ414
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

Medical convenience kits are used in various healthcare settings for procedures requiring sterile swabs. These kits are purchased by healthcare providers to ensure patient safety during medical treatments.

Why This Is Dangerous

An open seal on the packaging of the BD ChloraPrep Triple Swabsticks may compromise sterility, increasing the risk of infection during medical procedures.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

The recall affects the availability of these medical kits, which are essential for maintaining sterility during procedures. Healthcare providers must ensure they have safe alternatives available.

Practical Guidance

How to identify if yours is affected

  1. Check the SKU number on the packaging.
  2. Verify if the kit is labeled as ANESTHESIA ARTLINE PACK, Kit SKU DYNJ47387B.
  3. Look for the affected model numbers: UDI/DI 10193489217070 and Lot Number 25EBJ414.

Where to find product info

The SKU number can typically be found on the outer packaging of the medical kit.

What timeline to expect

Expect refund processing to take 4-6 weeks after returning the product.

If the manufacturer is unresponsive

  • Document all communication attempts with Medline.
  • Contact the FDA if the company remains unresponsive.

How to prevent similar issues

  • Always check for seals and packaging integrity before use.
  • Purchase from reputable suppliers to ensure product safety.
  • Stay updated on recalls involving medical devices.

Documentation advice

Keep a record of your purchase, including receipts, and document any correspondence regarding the recall.

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Product Details

The recall includes Medline medical convenience kits packaged as ANESTHESIA ARTLINE PACK, Kit SKU DYNJ47387B. The affected model numbers include UDI/DI 10193489217070 and Lot Number 25EBJ414.

Key Facts

  • Recall date: December 24, 2025
  • Total kits recalled: 120
  • Affected model numbers: UDI/DI 10193489217070, Lot Number 25EBJ414
  • No injuries reported at this time

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 10193489217070
Lot Number 25EBJ414
Affected States
ALL
Report Date
February 18, 2026
Recall Status
ACTIVE

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