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Medline Recalls Adhesive Bandages Over Sterility Concerns

Medline Industries recalled 1.57 million units of Curad Touch-Free and Quick-Strip Bandages on October 27, 2025. The packaging may exhibit open seals, compromising sterility. Consumers should stop use immediately and follow the recall instructions provided by the manufacturer.

Official notice
Medline Industries, LPHealth & Personal CareMedical DevicesUDI/DI 30888277715947 (each)10888277715943 (box)20888277715940 (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 30888277715947 (each), 10888277715943 (box), 20888277715940 (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

Fur Friends Plastic Sterile Adhesive Bandages are primarily used for minor cuts and scrapes. Consumers, including parents and caregivers, purchase these products for first-aid kits or home use.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers should stop using the affected bandages to avoid potential health risks. This recall may cause inconvenience as consumers will need to replace their bandages.

Practical Guidance

How to identify if yours is affected

  1. Check the packaging for the Medline Item Number NON256133QS.
  2. Look for any visible signs of open seals in the packaging.
  3. Verify the recall notice on the FDA website for additional details.

Where to find product info

The Medline item number and other identifiers are typically found on the box or individual bandage packaging.

What timeline to expect

Expect a refund or replacement to process within 4-6 weeks after returning the product.

If the manufacturer is unresponsive

  • Document your communication attempts with Medline.
  • Consider filing a complaint with the FDA if you do not receive a response.

How to prevent similar issues

  • Always check packaging for integrity before purchase.
  • Look for products with clear labeling and safety certifications.
  • Research recalls on products before use.

Documentation advice

Keep receipts, correspondence with the manufacturer, and any photos of the product as records.

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Product Details

The recalled product is Fur Friends Plastic Sterile Adhesive Bandages, 0.75" x 3", with Medline Item Number NON256133QS. The recall encompasses all lots of the Curad Touch-Free and Quick-Strip Bandages. These products were distributed in the US, Guam, Canada, and the United Arab Emirates.

Key Facts

  • Recall date: October 27, 2025
  • Quantity recalled: 1,566,500 units
  • Distribution: US, Guam, Canada, UAE
  • Hazard classification: Class II

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 30888277715947 (each)
10888277715943 (box)
20888277715940 (case)
ALL LOTS
Report Date
December 17, 2025
Recall Status
ACTIVE

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