Recall one batch of SINERGINA 100 MG TABLET
2026-02-05
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
التصنيف
التاريخ
2025-08-11
اسم المستحضر
SINERGINA 100 MG TABLET
اجراء الاستدعاء
مستوى الاستدعاء
نوع المستحضر
سبب السحب
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.
التوصيات
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).
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