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Medline Recalls Adhesive Bandages Over Sterility Concerns

Medline Industries recalled 6,989,900 units of Quick Strip Fabric Sterile Adhesive Bandages on October 27, 2025. The recall stems from open seals in the packaging that may compromise sterility. Patients and healthcare providers should stop using these products immediately.

Official notice
Medline Industries, LPHealth & Personal CareMedical DevicesUDI/DI 10888277699410 (each)20888277699417 (box)30888277699414 (case)

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
October 27, 2025
Status
ACTIVE
Severity
8/10

Quick Facts at a Glance

Recall Date
October 27, 2025
Hazard Level
HIGH
Brand
Medline Industries, LP
Category
Health & Personal Care
Sold At
Multiple Retailers
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
Adhesive Bandages
Model numbers
UDI/DI 10888277699410 (each), 20888277699417 (box), 30888277699414 (case), ALL LOTS
Sold at
Multiple Retailers

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    October 27, 2025

  2. Reported by FDA DEVICE

    December 17, 2025

  3. RecallRadar source check

    December 24, 2025

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.

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

Quick Strip Fabric Sterile Adhesive Bandages are commonly used for minor cuts and wounds. They provide a sterile barrier that helps prevent infections.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers must stop using these bandages to avoid potential health risks. The inconvenience of returning the product and finding alternatives may be significant.

Practical Guidance

How to identify if yours is affected

  1. Check the product packaging for the Medline Item Number NON25650QS.
  2. Inspect for any open seals in the packaging.
  3. Review purchase records to confirm if you have the affected product.

Where to find product info

The Medline Item Number can be found on the product packaging, typically on the back or side.

What timeline to expect

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

If the manufacturer is unresponsive

  • Contact Medline Industries customer service again.
  • Keep a record of your communication attempts.

How to prevent similar issues

  • Always check the seals on medical products before use.
  • Look for certifications indicating sterility.

Documentation advice

Document any correspondence with Medline regarding the recall, including dates and details of conversations.

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Product Details

The recalled products are Quick Strip Fabric Sterile Adhesive Bandages, measuring 0.75" x 3", with Medline Item Number NON25650QS. They were distributed in the United States, Guam, Canada, and the United Arab Emirates.

Key Facts

  • Recall date: October 27, 2025
  • Quantity: 6,989,900 units recalled
  • Hazard: Compromised sterility due to open seals
  • Affected regions: US, Guam, Canada, UAE

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 10888277699410 (each)
20888277699417 (box)
30888277699414 (case)
ALL LOTS
Report Date
December 17, 2025
Recall Status
ACTIVE

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