HIGHFDA DRUG

Rite Aid Alcohol Prep Pads Recalled Over Subpotent Isopropyl Alcohol Levels (2025)

Rite Aid alcohol prep pads distributed nationwide are recalled after subpotent isopropyl alcohol levels were found below label concentration. Medline Industries, LP notified distributors and healthcare providers in a Class II recall dated July 7, 2025. Consumers and healthcare providers should stop using the product immediately and seek guidance from a healthcare provider.

Official notice

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DRUG
Recall date
July 7, 2025
Status
ACTIVE
Severity
8/10

Quick Facts at a Glance

Recall Date
July 7, 2025
Hazard Level
HIGH
Brands
Rite Aid, Alcohol (ALCOHOL), Medline Industries
Category
Health & Personal Care
Sold At
Unknown
Geographic Scope
1 states
At-Risk Groups
GENERAL, PREGNANT, PETS

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 - Drug Safety; 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
Rite Aid, Alcohol (ALCOHOL), Medline Industries
Product type
Isopropyl Alcohol Prep Pads
Model numbers
61224070083
UPC codes
11822-5156, 11822-5156-6, 11822-5156-2, 6122407008
Sold at
Unknown
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    July 7, 2025

  2. Reported by FDA DRUG

    September 3, 2025

  3. RecallRadar source check

    April 18, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

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

About This Product

First aid alcohol prep pads used to clean wounds or surfaces prior to procedures. Labeled alcohol concentration is essential for antiseptic effectiveness.

Why This Is Dangerous

If the isopropyl alcohol concentration is below labeling, the pads may not disinfect effectively, potentially increasing infection risk.

Industry Context

This recall is not part of a broader industry pattern at this time.

Real-World Impact

Patrons in clinical and home settings should switch to a different brand or product with properly labeled concentration.

Practical Guidance

How to identify if yours is affected

  1. Locate packaging for NDC 11822-5156-2
  2. Check model 61224070083 on the package
  3. Verify lot numbers if present on packaging

Where to find product info

FDA enforcement page and Medline Industries notification

What timeline to expect

Replacement or refund processes will be communicated by the distributor in the coming weeks

If the manufacturer is unresponsive

  • Document all contact attempts
  • Escalate to FDA Consumer Complaint Coordinators if supplier is non-responsive
  • Consider filing a consumer complaint with CPSC if concerned about medical devices or supplies

How to prevent similar issues

  • Verify NDC codes before purchase
  • Choose reputable brands with clear potency testing
  • Keep a small supply of antiseptic wipes from multiple brands for home use
  • Ask for potency certification or COA when buying medical-grade products

Documentation advice

Keep packaging, recall notices, and all correspondence; photograph product and UPC/NDC code on packaging

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Product Details

Model: 61224070083. Brand: ALCOHOL. Distributor: Rite Aid. Quantity: 984,000 pads. National distribution. NDC: 11822-5156-2. Status: Active as of recall date.

Reported Incidents

No specific injuries or incidents are listed in the recall notice. The enforcement report references a subpotent potency issue, not reported injuries.

Key Facts

  • Class II recall
  • High hazard level
  • Active recall as of 2025-09-03

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
GENERALPREGNANTPETSPREGNANT
Injury Types
POISONINGELECTRICAL

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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