Recall of Daroxime 500 MG FCT batches produced by DAR ALDAWA Manufacturer
2026-02-12
الاسم التجاري الاسم العلمي رقم التسجيل رقم التشغيلة المتأثرة الشركة الصانعة Trade Name Scientific Name Register Number Affected batch number Manufacturer Daroxime 500 MG FCT CEFUROXIME AXETIL 2210234368 3668 3669 1483 4156 3670 0266 0264 0263 0262 0267 0265 DAR ALDAWA
التصنيف
ملف
التاريخ
2025-10-26
اسم المستحضر
Daroxime 500 MG FCT
اجراء الاستدعاء
مستوى الاستدعاء
نوع المستحضر
سبب السحب
SFDA has issued a recall of Daroxime 500 MG FCT batches due to noncompliance with Registered specifications. The company requested voluntary recall of the effected batches.
التوصيات
For healthcare professionals: Stop dispensing the affected batches immediately. Embargo/Quarantine all remaining stock. Affected batches 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 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).
评论与建议
如对政府服务有任何咨询或意见,请填写所需信息。