HIGH

Medline Recalls Alcohol Prep Pads Due to Subpotency Risk

Medline Industries recalled 222,800 boxes of alcohol prep pads on September 29, 2025. The recall follows concerns the product may not meet potency standards. Consumers must stop using the pads and seek guidance from healthcare providers.

Quick Facts at a Glance

Recall Date
September 29, 2025
Hazard Level
HIGH
Brand
Medline Industries, LP
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

Hazard Information

Subpotent Drug

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact Medline Industries, LP or your healthcare provider for guidance. Notification method: Letter

Product Details

The recall affects Medline Alcohol Prep Pads, 2-Ply Pad, containing 70% Isopropyl Alcohol. Each box contains 100 pads, and there are 10 boxes per case, totaling 1,000 pads per case. They were distributed nationwide in the United States.

The Hazard

The recalled alcohol prep pads are classified as a subpotent drug. This means the pads may not effectively disinfect skin as intended, posing a risk during medical procedures.

Reported Incidents

There are no specific reported incidents or injuries associated with this recall. The potential for ineffective disinfection raises concerns for users.

What to Do

Consumers and healthcare providers should stop using the recalled alcohol prep pads immediately. They can contact Medline Industries, LP for further guidance.

Contact Information

For more information, consumers can visit Medline's website or call the company directly at the contact number provided in their notification letter.

Key Facts

  • 222,800 units recalled
  • Manufactured for Medline Industries, LP
  • Subpotent risk may affect disinfecting ability
  • Immediate action required by consumers

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
Lot #: 61224040057
Affected States
ALL
Report Date
October 29, 2025
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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