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Lower risk Drug recall · FDA · Published July 7, 2025

Medline Alcohol Prep Pads Recall: Subpotent Isopropyl Alcohol Levels

Medline Industries recalls Good Neighbor Pharmacy Alcohol Prep Pads due to subpotent isopropyl alcohol levels below labeled concentration. Consumers should check product details and contact Medline for guidance.

🇺🇸 FDA recall #D-0604-2025DrugMedline Industries ›
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Recalling firmMEDLINE INDUSTRIES, LP - Northfield3 Lakes Dr · Northfield, IL 60093-2753
✎ GovInfoNow plain-language explainer

What happened, in plain English

Medline Industries recalls Good Neighbor Pharmacy Alcohol Prep Pads because the isopropyl alcohol concentration is lower than labeled. This could lead to ineffective disinfection, potentially increasing infection risk during use. Read more at govinfonow.com/recall/31996-medline-alcohol-prep-pads-recall-subpotent-isopropyl-alcohol-levels.

Source Summary by GovInfoNow · govinfonow.com/recall/31996-medline-alcohol-prep-pads-recall-subpotent-isopropyl-alcohol-levels · Updated August 17, 2026 · FDA enforcement record: FDA #D-0604-2025

Cite this page

“Medline Alcohol Prep Pads Recall: Subpotent Isopropyl Alcohol Levels.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/31996-medline-alcohol-prep-pads-recall-subpotent-isopropyl-alcohol-levels. Based on FDA recall #D-0604-2025 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0604-2025%22&limit=1).

Why it’s dangerous

The pads contain less isopropyl alcohol than labeled, meaning they may not disinfect properly. This could lead to incomplete cleaning and potential infection risks, especially in medical or high-touch environments.

Who’s affected

People who purchased Good Neighbor Pharmacy Alcohol Prep Pads from pharmacies or retailers. Those using the pads for disinfection are most at risk of ineffective cleaning.

How to tell if you have this one

Check for the product name 'Good Neighbor Pharmacy Alcohol Prep Pads' on the packaging. The NDC code 46122-043-78 or 61224070074 is listed on the box. These pads were distributed by AmeriSource Bergen in Conshohocken, PA.

  • Brand
    Medline Industries
  • Category
    Drug
FDA recall event · 6 products

All 6 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Ongoing
  • Distribution
    Nationwide
Recall numberProduct, codes & lotsQuantityNDC
D-0600-2025Medline Alcohol Prep Pads, 70% Isopropyl Alcohol, 100 Sterile 2-Ply Pads, Single Use Only, Large, www.medline.com, Manufactured for Medline Industries, LP, Three Lakes Drive, Northfield, IL 60093 USA, 1-800-MEDLINE, NDC 53329-811-30.; 612240400576669874 swabs53329-811-30, 53329-811-09, 6122404005
D-0601-2025CURAD Alcohol Prep Pads, Sterile, Medium, 2-Ply, Contents: 5 boxes per Carton, 30 Boxes per Case, Single Use Only, Manufactured for Medline Industries, LP, Three Lakes Drive, Northfield, IL 60093, USA, Made in India, www.curad.com, 1-800-633-5463, NDC 53329-827-30; 612240500021,639,996 pads53329-827-60, 53329-827-36, 53329-827-30, 53329-827-29, 53329-827-40, 53329-827-09, 53329-827-33, 6122405000
D-0602-2025ReliOn, Sterile Alcohol Swabs, Skin Cleanser, 200 Swabs, Distributed by, Walmart, Inc., Bentonville, AR 72716 Walmart: 200 eaches per box, 24 boxes per case (4,800 eaches per case), NDC 49035-814-60.; 612240700733,456,000 pads49035-814-30, 49035-814-60, 6122407007
D-0603-2025H-E-B, inControl, Sterile* Alcohol Pads, CONT. 100 PADS, Packaged in China with components from Taiwan, Elaborado Con Orgullo Y Cuidado PARA H-E-B, San Antonio, TX 78204, NDC 37808-809-09.; 61224080041300000 pads37808-809-30, 37808-809-60, 37808-809-09, 6122408004
D-0604-2025Good Neighbor Pharmacy, Alcohol Prep Pads, Distributed By AmeriSource Bergen, 1 West First Avenue, Conshohocken, PA 19428, Made in China: 100 eaches per box, 30 boxes per case, (3,000 eaches per case), NDC 46122-043-78.; 6122407007466,000 pads46122-043-78, 6122407007
D-0605-2025RITE AID PHARMACY, first aid alcohol prep pads, DISTRIBUTED BY: RITE AID. 200 NEWBERRY COMMONS, ETTERS, PA 17319, NDC 11822-5156-2.; 61224070083984,000 pads11822-5156-6, 11822-5156-2, 6122407008
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the NDC code 46122-043-78 or 61224070074 on the packaging to confirm if the product is recalled.

Where it went and when

Where it was distributed

Distributed nationwide.

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: yesFL

FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 58 days after the firm started it.

1. Firm started the recall: Jul 7, 202512. FDA classified it Class II: Aug 26, 202523. Published in FDA’s Enforcement Report: Sep 3, 202532025
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report

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-0604-2025 (July 7, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0604-2025 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