Wuxi Medical lnstrument Factory Co., Ltd.: Drug Recall

Recall #D-0247-2025 · 02/12/2025

Class II: Risk

Recall Details

Recall Number
D-0247-2025
Classification
Class II
Product Type
Drug
Recalling Firm
Wuxi Medical lnstrument Factory Co., Ltd.
Status
Ongoing
Date Initiated
02/12/2025
Location
Wuxi, N/A, China
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
37,500 Boxes

Reason for Recall

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

Product Description

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.

Distribution Pattern

FL

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.