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Medline Recalls Suture Removal Trays Due to Seal Failure

Medline Industries, LP recalled 2,448 Suture Removal Trays on December 24, 2025. The recall affects kits containing BD ChloraPrep Triple Swabsticks with potentially open seals. The company urges immediate cessation of use to avoid potential hazards.

Official notice
Medline Industries, LPHealth & Personal CareMedical DevicesUDI/DI 10195327379308Lot Number 25EBO576

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
7/10

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
Suture Removal Tray
Model numbers
UDI/DI 10195327379308, Lot Number 25EBO576
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 Suture Removal Tray is used in medical settings for removing sutures safely and effectively. Consumers purchase these kits for both professional healthcare use and home care.

Why This Is Dangerous

The open seal on the BD ChloraPrep Triple Swabsticks can lead to contamination, compromising patient safety. Users may unknowingly apply a non-sterile product, increasing the risk of infection.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers should stop using these kits immediately to prevent potential health risks. The recall may cause delays in treatment for those relying on these kits.

Practical Guidance

How to identify if yours is affected

  1. Check the SKU DYNDR1277A on the packaging.
  2. Look for Lot Number 25EBO576 on the product.
  3. Verify the UDI/DI 10195327379308 against the recall list.

Where to find product info

You can find the SKU and Lot Number on the outer packaging or the product insert.

What timeline to expect

Expect a refund or replacement process to take approximately 4-6 weeks.

If the manufacturer is unresponsive

  • Document your communication attempts with Medline.
  • Contact your healthcare provider for assistance.
  • File a complaint with the FDA if necessary.

How to prevent similar issues

  • Examine packaging for integrity before purchase.
  • Choose products from reputable manufacturers with good safety records.
  • Stay informed about recalls in the medical product category.

Documentation advice

Keep a record of your purchase, including receipts and any correspondence related to the recall.

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Product Details

The recalled product is the Suture Removal Tray, Kit SKU DYNDR1277A, with UDI/DI 10195327379308 and Lot Number 25EBO576. These kits were distributed nationwide in the United States.

Key Facts

  • Recall date: December 24, 2025
  • Quantity recalled: 2,448 kits
  • Affected packaging may compromise sterility
  • No reported injuries or incidents
  • Contact Medline for further instructions

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
7/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
UDI/DI 10195327379308
Lot Number 25EBO576
Affected States
ALL
Report Date
February 18, 2026
Recall Status
ACTIVE

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