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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Drug
Medications & Supplements/Topical Products

Medline and CURAD Alcohol Prep Pads Recalled for Subpotency

Agency Publication Date: March 20, 2025
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Summary

Medline Industries, LP has recalled approximately 8,309,870 Medline and CURAD brand Alcohol Prep Pads because they are subpotent. These sterile 2-ply pads, intended for single-use skin preparation before injections or minor procedures, may not contain the required concentration of alcohol to effectively disinfect the skin. Consumers should stop using these specific lots and contact a healthcare provider if they have concerns about potential infections.

Risk

Subpotent alcohol pads may fail to properly kill germs on the skin, which can lead to localized or systemic infections when the skin is subsequently punctured for an injection or medical procedure.

What You Should Do

  1. This recall affects Medline Alcohol Prep Pads (Large, NDC 53329-811-30) with lot 61224040057 and CURAD Alcohol Prep Pads (Medium, NDC 53329-827-30) with lot 61224050002.
  2. Stop using the recalled alcohol prep pads immediately as they may not provide adequate disinfection.
  3. If you have health concerns, contact your healthcare provider or pharmacist.
  4. Return any unused product to the place of purchase for a refund, throw it away, or contact Medline Industries, LP at 1-800-MEDLINE or 1-800-633-5463 for further instructions.
  5. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Medline Alcohol Prep Pads, 70% Isopropyl Alcohol (100 Sterile 2-Ply Pads)
Variants: Large, Single Use Only
Model:
MDS090670
Lot Numbers:
61224040057
NDC:
53329-811-30

Quantity: 6,669,874 pads

Product: CURAD Alcohol Prep Pads, Sterile (5 boxes per Carton, 30 Boxes per Case)
Variants: Medium, 2-Ply, Single Use Only
Model:
CUR090737RB
Lot Numbers:
61224050002
NDC:
53329-827-30

Quantity: 1,639,996 pads

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96404
Status: Active
Manufacturer: MEDLINE INDUSTRIES, LP - Northfield
Sold By: medline.com; curad.com
Manufactured In: United States, India
Units Affected: 2 products (6,669,874 pads; 1,639,996 pads)
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.