HIGH

Rite Aid Recalls Alcohol Prep Pads Due to Subpotency Hazard

Rite Aid recalled 984,000 first aid alcohol prep pads on July 7, 2025, due to subpotent isopropyl alcohol levels. The affected product may not effectively disinfect, posing health risks to users.

Quick Facts at a Glance

Recall Date
July 7, 2025
Hazard Level
HIGH
Brands
Rite Aid Corporation, ALCOHOL
Category
Health & Personal Care
Sold At
REI, Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL

Hazard Information

Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact MEDLINE INDUSTRIES, LP - Northfield or your healthcare provider for guidance. Notification method: Letter

Product Details

The recall affects Rite Aid first aid alcohol prep pads, model number 61224070083. These pads were distributed nationwide.

The Hazard

The alcohol prep pads contain isopropyl alcohol levels that fall below the labeled concentration. This subpotency can reduce effectiveness in disinfecting wounds.

Reported Incidents

No injuries or adverse events related to the recalled pads have been reported at this time. The hazard is classified as high due to potential health risks.

What to Do

Consumers should immediately stop using the affected product. Contact Medline Industries, LP or your healthcare provider for further guidance.

Contact Information

For more information, visit the FDA's recall page or contact Medline Industries at their Northfield address.

Key Facts

  • Quantity recalled: 984,000 pads
  • Recall date: July 7, 2025
  • No reported injuries or deaths
  • Distributed nationwide

Safety Assessment

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

Product Classification

Product TypeFirst Aid Alcohol Prep Pads
Sold At
REIMultiple Retailers

Product Details

Model Numbers
61224070083
UPC Codes
11822-5156
11822-5156-6
11822-5156-2
+1 more
Affected States
ALL
Report Date
September 3, 2025
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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