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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.

Official notice
Medline Industries, LPHealth & Personal CareMedical DevicesUDI/DI 10195327379292Lot Number 25EBJ785

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 10195327379292, Lot Number 25EBJ785
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 Sterile Resection Pack is commonly used in medical procedures to maintain sterility and prevent infections. Healthcare providers rely on these kits for their essential components during patient care.

Why This Is Dangerous

The open seal on the BD ChloraPrep Triple Swabsticks can lead to contamination, posing a risk of infection during medical procedures.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Patients and healthcare providers must stop using the affected kits to avoid the risk of infection, which can lead to serious health complications.

Practical Guidance

How to identify if yours is affected

  1. Check the SKU DYNDL1980A on the packaging.
  2. Verify the lot number 25EBJ785 if applicable.
  3. Confirm the product is from the recall notice.

Where to find product info

The SKU and lot number can typically be found on the product packaging or label.

What timeline to expect

Expect a response regarding refunds or replacements within 4-6 weeks of contacting Medline.

If the manufacturer is unresponsive

  • Document all correspondence with Medline.
  • Follow up via phone or email.
  • Consider filing a complaint with the FDA if issues persist.

How to prevent similar issues

  • Always inspect medical kits for damaged or open seals before use.
  • Purchase from reputable suppliers to ensure product integrity.
  • Verify that products have up-to-date certifications and are not expired.

Documentation advice

Keep records of your purchase, photos of the product, and any communication with Medline for future reference.

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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.

Key Facts

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

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 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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