HIGH

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.

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

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

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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.

The Hazard

The bandages may have open seals in the packaging, which can compromise their sterility. Using these bandages can lead to infection or other complications.

Reported Incidents

Currently, there are no reported injuries or incidents associated with the use of the recalled bandages. Medline issued the recall as a precautionary measure.

What to Do

Stop using the recalled bandages immediately. Contact Medline Industries or your healthcare provider for further instructions on how to return the product.

Contact Information

For more information, contact Medline Industries, LP at the phone number provided in the recall instructions. Visit the FDA website for details at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=Z-0902-2026.

Key Facts

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

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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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