Medline Industries recalls 100-pad alcohol pads sold in H-E-B and inControl stores due to subpotent isopropyl alcohol levels below labeled concentration. Consumers should check product details and contact Medline for remedies.
Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
Medline Industries is recalling 100-pad alcohol pads sold in H-E-B and inControl stores because the isopropyl alcohol concentration is lower than labeled. This could mean the pads are less effective for disinfection.
The alcohol pads contain less isopropyl alcohol than labeled, which means they may not disinfect as effectively. This could lead to less protection against germs, but does not pose a direct physical hazard like burns or injury.
H-E-B and inControl store customers who purchased the 10:00 pads packaged in China with components from Taiwan. People using these pads for disinfection may be at risk of reduced effectiveness.
Check for the product name 'Sterile* Alcohol Pads' with 100 pads, packaged in China with components from Taiwan. The NDC code 37808-809-09 or 61224080041 may help identify the product.
Look for the product name 'Sterile* Alcohol Pads' with 100 pads, packaged in China with components from Taiwan, and NDC code 37808-809-09 or 61224080041.
The alcohol pads have subpotent isopropyl alcohol levels below the labeled concentration, which may reduce their disinfection effectiveness.
Check for the product name 'Sterile* Alcohol Pads' with 100 pads, packaged in China with components from Taiwan, and NDC code 37808-809-09 or 61224080041.
The recall record does not specify a remedy, so contact Medline Industries for further instructions.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall D-0603-2025 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall D-0603-2025 from Medline Industries. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
