Wuxi Medical lnstrument Factory Co., Ltd.

FDA Initiates Class II Recall for Wuxi Medical Instrument Factory's ViaMed Alcohol Prep Pads Due to Sterility Concerns

Wuxi Medical Instrument Factory Co., Ltd. faces an FDA Class II recall for ViaMed Alcohol Prep Pads due to sterility assurance failures and cGMP deviations. This impacts Rece International Corp. and necessitates immediate supply chain review for sterile medical devices. Procurement and regulatory teams must assess exposure and reinforce supplier qualification protocols to mitigate risk.