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Medical Devices Sector
قطاع الأجهزة الطبية
المركز الوطني لبلاغات الأجهزة والمنتجات الطبية
mdprc 162 03 16 000
Becton Dickinson & Co. (BD)
BD Angiocath TM AutoguardTM shielded IV Catheter
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.
-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.
Becton Dickinson B.V.
Source Ref. Number:
SFDA urges all hospitals that have devices subjected to recall, to contact the company.
Becton Dickinson & Co. (BD).pdf
Copyright © 2008 Saudi Food and Drug Authority. All rights reserved.