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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 002 06 11 000
Date submitted: 6/1/2011
Manufacturer:bioMerieux Inc
Device Type:Slidex Staph Kits, Reagents
Description:Reagents, Microbiology, Bacteria, Identification, Staphylococcus aureus
Medical Device Identifier:Reference Nos: 73112, 73113 Lot Nos. 1007103196, 1007103197 Expiration Date: APR 22 2011
Reason of Field Safety Corrective Action:May Yield False-Negative Results
Remedy Action:Identify, isolate, and destroy any affected product in your inventory.
Athorized Representative/Importer/Distributor:Fuad Abdul Jalil Al Fadhli & Sons, Riyadh (01) 4550807
Report Source:NCMDR
Source Ref. Number:67EA13E74C297
SFDA Comments:SFDA urges all hospitals that have devices subjected to recall, to contact the company
Attachments:No Attachments