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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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High RiskFDA Drug
Medications & Supplements/Topical Products

Webcol Alcohol Prep Pads Recalled for Microbial Contamination

Agency Publication Date: March 16, 2026
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Summary

Cardinal Health 200, LLC is recalling approximately 174.4 million Webcol Alcohol Prep Pads due to potential microbial contamination. The affected 2-ply sterile pads, sold in 200-count boxes, were found to contain Paenibacillus phoenicis, rendering the product non-sterile. This discovery was made after testing confirmed the presence of the contaminant in affected lots.

Risk

The use of these non-sterile prep pads may pose a potential infection risk, especially to vulnerable groups or individuals with weakened immune systems. A contaminant like Paenibacillus phoenicis can lead to serious health complications if it enters a wound or the bloodstream during medical procedures.

What You Should Do

  1. Check the lot number printed on your Webcol Alcohol Prep Pad packaging to see if your product is included in this recall.
  2. See the Affected Products section below for the full list of affected codes.
  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 the manufacturer 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: Webcol Alcohol Prep pad (70% isopropyl alcohol) 2 ply, 200 count boxes
Variants: 2 ply, 200 count
Lot Numbers (453):
25K064362
25K064762
25K064962
25K065762
25K066062
25K079662
25K079762
25K079862
25K080862
25K080762
25K081962
25K082062
25L013962
25L015162
25K080662
25K081662
25K081762
25K081862
25L014262
25L015762
25G045062
25L014462
25L014562
25L014662
25L014762
25L014862
25L014962
25L015062
25L016162
25L028262
25L028362
25L029462
25L028462
25L028562
25L028662
25L028762
25L029562
25L028862
25L028962
25L029062
25L029662
25L029762
25L029362
25L044562
25L044062
25L044162
25L044762
25L044862
25L045262
25L055962

Manufacturer: Cardinal Health 200, LLC, 3651 Birchwood Drive, Waukegan, IL 60085.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98503
Status: Active
Manufacturer: Cardinal Health 200, LLC
Sold By: medical suppliers; hospitals; pharmacies
Manufactured In: United States
Units Affected: 174,380,282 units
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.