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Medical Devices Sector
قطاع الأجهزة الطبية
NCMDR
National Center for Medical Devices Reporting
المركز الوطني لبلاغات الأجهزة والمنتجات الطبية
NCMDR Recall
Reference Number: mdprc 028 11 11 000
Date submitted: 11/9/2011
Manufacturer:Professional Disposables International (PDI)
Device Type:Single-use, Antiseptic, Nonsterile Alcohol Prep Pads
Description:Personal, Antiseptic
Medical Device Identifier:Catalog Num:C29600 PR100
Reason of Field Safety Corrective Action:May contain low levels of Bacillus cereus.
Remedy Action:Remove the product identified from the market and return to the Manufacturer / Distributor.
Athorized Representative/Importer/Distributor:Medical Oasis International Riyadh 01 4050925
Report Source:NCMDR
Source Ref. Number:2B4244DF461D6
SFDA Comments:SFDA urges all hospitals that have devices subjected to recall, to contact the company.
Attachments:No Attachments