OK Your changes have been successfully saved
SFDA Home Page
Medical Devices Sector
قطاع الأجهزة الطبية
National Center for Medical Devices Reporting
المركز الوطني لبلاغات الأجهزة والمنتجات الطبية
NCMDR Recall
Reference Number: mdprc 162 03 16 000
Date submitted: 3/24/2016
Manufacturer:Becton Dickinson & Co. (BD)
Device Type:BD Angiocath TM AutoguardTM shielded IV Catheter
Description:Catheter, Single-use
Medical Device Identifier:Catalog Number 381700
Reason of Field Safety Corrective Action:The device may have a defect in the catheter. In some instances this defect could result in catheter separation or breakage.
Remedy Action:-Immediately review your inventory for the specific Catalog (Ref) and lot numbers listed in Attachment A, and quarantine product subject to the recall. Immediately discontinue the shipment of the affected product.

-Upon receipt of the Notice of Return BD will contact you to organize the replacement of the recalled product at no charge.
Athorized Representative/Importer/Distributor:Becton Dickinson B.V.
Report Source:NCMDR
Source Ref. Number:C3CAEA89F43F4
SFDA Comments:SFDA urges all hospitals that have devices subjected to recall, to contact the company.
Attachments: Becton Dickinson & Co. (BD).pdf