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Medline Recalls Adhesive Bandages Over Sterility Concerns

Medline Industries recalled 1,725,600 units of Quick Strip Plastic Sterile Adhesive Bandages due to potential packaging defects. The recall, issued on October 27, 2025, affects all lots of Curad Touch-Free and Quick-Strip Bandages. Open seals may compromise the sterility of the product, posing a health risk.

Official notice
Medline Industries, LPHealth & Personal CareMedical DevicesUDI/DI 10888277699397 (each)20888277699394 (box)30888277699391 (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 10888277699397 (each), 20888277699394 (box), 30888277699391 (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 Plastic Sterile Adhesive Bandages are used for covering minor cuts and abrasions. These bandages are popular among consumers for their convenience and ease of use in first-aid applications.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

Consumers using these bandages may face serious health risks if they are not sterile. This recall necessitates immediate action to ensure safety.

Practical Guidance

How to identify if yours is affected

  1. Check the packaging for the item number NON25500QS.
  2. Inspect for any open seals or compromised packaging.
  3. Verify if the bandages were purchased from a recalled lot.

Where to find product info

Look for the item number on the back of the packaging or box.

What timeline to expect

Expect refund processing to take approximately 4-6 weeks.

If the manufacturer is unresponsive

  • Contact Medline customer service again for follow-up.
  • Document your communications and attempts to resolve the issue.
  • Consider filing a complaint with the FDA if you receive no response.

How to prevent similar issues

  • Always check packaging integrity before use.
  • Look for safety certifications on medical products.
  • Avoid purchasing from unverified retailers.

Documentation advice

Keep records of your purchase, including receipts and any correspondence with Medline.

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Product Details

The recalled product is Quick Strip Plastic Sterile Adhesive Bandages, measuring 0.75 inches by 3 inches. The Medline item number is NON25500QS. These bandages were distributed throughout the US, Guam, Canada, and the United Arab Emirates.

Key Facts

  • Recall date: October 27, 2025
  • Distribution: US, Guam, Canada, UAE
  • Class II recall due to sterility risk
  • Stop using affected bandages immediately

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 10888277699397 (each)
20888277699394 (box)
30888277699391 (case)
ALL LOTS
Report Date
December 17, 2025
Recall Status
ACTIVE

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