Recall batches of SABRIL 500MG F.C.TAB
2023-07-21Product Description :
الاسم التجاري |
الاسم العلمي |
رقم التسجيل |
رقم التشغيلة المتأثرة |
الشركة الصانعة |
Trade Name |
Scientific Name |
Register Number |
Affected batch number |
Manufacturer |
Vigabatrin 500 Mg |
25-883-19 |
2006B 2988D 2989A 2990D |
sanofi-aventis |
Issue :
Saudi FDA issued Recall four batches of SABRIL 500MG F.C.TAB due to) Tiapride (cross Contamination. Sanofi-Aventis is voluntarily recalling the affected batches.
Recommendations :
For healthcare professionals, Stop dispensing the above batches immediately. Embargo/Quarantine all remaining stock. Affected batch should be returned to the supplier.
For patients,
- Consult your healthcare provider prior to discontinuing use of the affected batches, or for any health concerns.
- Contact the recalling firm or Saudi FDA if you have any questions about the recall.
- Adverse reactions or quality problems experienced with the use of this product may be reported to Saudi Vigilance either online or call center (Call 19999).