21 June 2021

Safety alerts

Reference: CIR-2021-00000095

To all health facilities / all health care practitioners in Dubai's private health sector

Referring to the above subject, DHA notifies all health facilities regarding the Circular issued by the MOHAP for perusal and adhere to what is stated

 

Medical Device Product Recall HeartWare Ventricular Assist Device (HVAD)™ System 

Medical Device Quality Notification Program Chip Urisys 1100 INT. SW 5.71 CAT # 8955433190

Voluntary manufacturer Recall of Medical Device Trilogy 100, Trilogy 200, Garbin Plus, Aeris, LifeVent, BiPAP V30, and BiPAP A30/A40 Series Device Models

Voluntary manufacturer Recall of number lots of Medical Device StimLoc™ Burr Hole Cover

 

 

Thanks in advance for your good co-operation

Drug Control Section

Health Regulation Sector

DHA

 

Supporting Documents:

تقارير السلامة للوسائل الطبية - HeartWare Ventricular Assist Device HVAD System - تعميم خارجي.pdf:

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تقارير السلامة للوسائل الطبية - Program Chip Urisys 1100 INT SW 5.71 - تعميم خارجي.pdf:

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- تقارير السلامة للوسائل الطبية - Trilogy 100 - Trilogy 200 - (002).pdf:

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تقارير السلامة للوسائل الطبية - StimLoc Burr Hole Cover -.pdf:

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