HIGH

CURAD Alcohol Prep Pads Recall for Subpotent Isopropyl Alcohol (2025)

CURAD Alcohol Prep Pads recalled nationwide after tests found isopropyl alcohol levels subpotent. Medline Industries is the maker listed on recall documents. The issue concerns diluted potency below labeled concentration. Stop using immediately and contact Medline for guidance.

Quick Facts at a Glance

Recall Date
July 7, 2025
Hazard Level
HIGH
Brands
CURAD, Medline Industries, LP
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL, PREGNANT, PETS

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

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About This Product

CURAD Alcohol Prep Pads are sterile, single-use pads used for sanitizing skin before injections or procedures. They are sold nationwide and manufactured for Medline by a production facility in India.

Why This Is Dangerous

Subpotent alcohol may not provide adequate antiseptic protection, potentially leading to infection risk in clinical settings.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

High in clinical use. Could affect wound cleaning and procedure prep, especially in settings with high infection-control standards.

Practical Guidance

How to identify if yours is affected

  1. Check NDC 53329-827-30 on packaging.
  2. Check model number 61224050002.
  3. Verify lot code and packaging details.

Where to find product info

Recall notice and curad.com/product-recall pages; packaging labels.

What timeline to expect

Refunds/replacements typically processed within several weeks; follow official instructions.

If the manufacturer is unresponsive

  • Document attempts to contact
  • Escalate to consumer protection agencies if needed
  • Consider credit card dispute if purchase is recent and unresolved.

How to prevent similar issues

  • In clinical purchases, verify potency certifications
  • Prefer suppliers with batch-level testing
  • Check NDC codes when stocking supplies
  • Maintain inventory segregation for recalled lots

Documentation advice

Keep recall notification, packaging images, purchase receipts, correspondence with Medline, and any incident records.

Product Details

Model: 61224050002. Sold nationwide. Quantity: 1,639,996 pads. Packaging: 5 boxes per carton, 30 boxes per case. Manufactured for Medline Industries LP, Three Lakes Drive, Northfield, IL 60093, USA. Made in India. NDC 53329-827-30. Website: www.curad.com. 1-800-633-5463.

Reported Incidents

No injuries or incidents have been reported in the recall notice.

Key Facts

  • 1,639,996 pads recalled
  • Model 61224050002
  • NDC 53329-827-30
  • Distrib. nationwide
  • Manufactured for Medline Industries, LP
  • Made in India
View Original Recall on FDA - Drug Safety

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Safety Guide

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Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERALPREGNANTPETS
Injury Types
LACERATIONBURNOTHER

Product Classification

Product TypeAlcohol Prep Pads
Sold At
Multiple Retailers

Product Details

Model Numbers
61224050002
UPC Codes
53329-827
53329-827-60
53329-827-36
+6 more
Affected States
ALL
Report Date
September 3, 2025
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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