US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Feb 12, 2025 (2 years ago)

ViaMed Alcohol Prep Pads, For External Use Only, 70% Isopropyl Alcohol, Sterile, 100…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Lack of assurance of sterility and cGMP deviations observed at the manufacturing site.

What was recalled

ViaMed Alcohol Prep Pads, For External Use Only, 70% Isopropyl Alcohol, Sterile, 100 pieces per Box, 100 boxes per Carton, Sterile, Manufactured by Wuxi Medical Instrument Factory Co., Ltd., Made in China, Manufactured for: Rece International Corp., Miami Lakes, FL, 33014, USA, NDC: 70006-500-01.

Recalling firm
Wuxi Medical lnstrument Factory Co., Ltd.
Origin
N/A, China
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0247-2025

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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