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Unrated Drug recall · FDA · Published March 2, 2026

Cardinal Health 200 Webcol Alcohol Prep Pads Recall: Microbial Contamination Risk

Cardinal Health 200 LLC recalls 200-count Webcol Alcohol Prep pads (70% isopropyl alcohol) due to microbial contamination with Paenibacillus phoenicis. Affected lots include specific batch numbers listed in the recall notice.

🇺🇸 FDA recall #D-0528-2026DrugCardinal Health 200 ›
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Recalling firmCardinal Health 200, LLC3651 Birchwood Dr · Waukegan, IL 60085-8337
✎ GovInfoNow plain-language explainer

What happened, in plain English

Cardinal Health 200 LLC is recalling 200-count Webcol Alcohol Prep pads (70% isopropyl alcohol) because they contain microbial contamination identified as Paenibacillus phoenicis. This could pose a health risk if the pads are used for medical purposes. Read more at govinfonow.com/recall/31467-cardinal-health-200-webcol-alcohol-prep-pads-recall-microbial-contamination.

Source Summary by GovInfoNow · govinfonow.com/recall/31467-cardinal-health-200-webcol-alcohol-prep-pads-recall-microbial-contamination · Updated August 17, 2026 · FDA enforcement record: FDA #D-0528-2026

Cite this page

“Cardinal Health 200 Webcol Alcohol Prep Pads Recall: Microbial Contamination Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/31467-cardinal-health-200-webcol-alcohol-prep-pads-recall-microbial-contamination. Based on FDA recall #D-0528-2026 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0528-2026%22&limit=1).

Why it’s dangerous

The pads were found to have microbial contamination from Paenibacillus phoenicis, a type of bacteria that can cause infections if introduced into wounds or open skin areas. This contamination occurred during manufacturing, potentially leading to health risks when the pads are used for medical purposes.

Who’s affected

People who own or use the recalled Webcol Alcohol Prep pads for medical purposes, particularly those in healthcare settings or home medical use. Individuals using the pads for disinfection may be at risk if the contamination leads to infection.

How to tell if you have this one

Check for the product name 'Webcol Alcohol Prep pads (70% isopropyl alcohol) 2 ply, 200 count boxes' from Cardinal Health 200 LLC. The affected lots are listed in the recall notice with specific batch numbers starting with '25H065362' through '25L015262'.

  • Brand
    Cardinal Health 200
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Lot Number

    Look for the lot number on the box, which is listed in the recall notice as specific batch numbers starting with '25H065362' through '25L015262'.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFLPuerto Rico: yesPR

FDA distribution: “Nationwide within the United States, Puerto Rico and Japan.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA published this recall 23 days after the firm started it.

1. Firm started the recall: Mar 2, 202612. Published in FDA’s Enforcement Report: Mar 25, 202623. FDA classified it Class I: May 11, 202632026
  1. Firm started the recall
  2. Published in FDA’s Enforcement Report
  3. FDA classified it Class I

Dates from the agency record only; steps without a date are left out.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #D-0528-2026 (March 2, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0528-2026 to see it in context.
  • Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA