Wuxi Medical Instrument Factory Co., Ltd. recalls ViaMed Alcohol Prep Pads due to lack of sterility assurance. Products may contain contaminants from manufacturing defects. Consumers should check lot numbers on packaging for affected batches.
Lack of assurance of sterility and cGMP deviations observed at the manufacturing site.
Wuxi Medical Instrument Factory Co., Ltd. is recalling ViaMed Alcohol Prep Pads because the manufacturing process failed to ensure sterility. This could mean the pads might be contaminated, posing a risk of infection if used externally.
The manufacturing process had issues that could lead to contamination. The pads might not be sterile as claimed, which means they could introduce harmful bacteria or other contaminants when applied to skin.
People who own or use ViaMed Alcohol Prep Pads for external wounds or skin disinfection. Those with open wounds or sensitive skin may be at slightly higher risk of infection.
Check the packaging for lot numbers: 200830 (expires 08/29/2025), 210925 (expires 09/24/2026), or 221225 (expires 12/24/2027). Products were sold in boxes of 100 pads, with 100 boxes per carton.
Look for lot numbers on the packaging: 200830, 210925, or 221225.
The recall is due to manufacturing defects that could mean the pads are not sterile. They should not be used until the recall is resolved.
Check the lot numbers on the packaging: 200830 (expires 08/29/2025), 210925 (expires 09/24/2026), or 221225 (expires 12/24/2027).
The recall does not specify a return or disposal action. Check the product lot number and contact the manufacturer if you have concerns.
We’ve drafted a message you can send ViaMed to request your refund or repair — edit it as you like.
Subject: Recall D-0247-2025 — ViaMed ViaMed Hello, I own a ViaMed that is covered by recall D-0247-2025 from ViaMed. 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.
