Medline recalls 100 sterile alcohol prep pads due to subpotent drug content. This means the product may not contain enough active ingredient for intended use. Consumers should check product details and contact Medline for guidance.
Subpotent Drug
Medline is recalling 100 sterile alcohol prep pads that may have insufficient active ingredient. This could mean the pads don't work as intended for disinfection. Affected customers should check their product details and contact Medline for instructions.
The product contains a subpotent drug, meaning it has less active ingredient than required. This could result in the pads being less effective for disinfection. The hazard does not involve immediate physical harm but affects the product's intended use.
People who own or use Medline's 100 sterile alcohol prep pads with the specific SKU MDS090670 and lot number 61224040057 are affected. Healthcare workers and others using these pads for disinfection are at higher risk.
Check for the SKU MDS090670 and lot number 61224040057 on the product packaging. These pads were sold online through Medline's website and manufactured in Northfield, IL.
Look for SKU MDS090670 and lot number 61224040057 on the packaging to confirm if you have the recalled item.
The product contains a subpotent drug, meaning it may have less active ingredient than required for intended use.
Check the product details to confirm if you have the recalled item. Contact Medline at 1-800-MEDLINE for further instructions.
The recall is for subpotent drug content, which affects the product's effectiveness, not immediate physical harm.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall D-0288-2025 — Medline Medline Hello, I own a Medline that is covered by recall D-0288-2025 from Medline. 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.
