Recall one batch of SINERGINA 100 MG TABLET
2025-08-11Product Description :
|
الاسم التجاري |
الاسم العلمي |
رقم التسجيل |
رقم التشغيلة المتأثرة |
الشركة الصانعة |
|
Trade Name |
Scientific Name |
Register Number |
Affected batch number |
Manufacturer |
|
SINERGINA 100 MG TABLET |
PHENYTOIN
|
Not registered
|
3241 |
FAESFARMA |
Issue :
The Saudi Food and Drug Authority (SFDA) has issued a recall of one batch of SINERGINA 100 MG TABLET due to the batch’s failure to comply with the conditions and requirements for obtaining a permit for pharmaceutical products.
Recommendations :
For healthcare professionals: Stop dispensing the affected batch 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 batch, or for any health concerns.
- Contact the recalling firm or SFDA 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).