Recall two batches of ROZEL 60MG INJ
2024-12-08
الاسم التجاري الاسم العلمي رقم التسجيل رقم التشغيلة المتأثرة الشركة الصانعة Trade Name Scientific Name Register Number Affected batch number Manufacturer ROZEL 60MG INJ DENOSUMAB غير مسجل 23120007 Intas Pharma 23120005
التصنيف
ملف
التاريخ
2024-09-15
اسم المستحضر
ROZEL
اجراء الاستدعاء
مستوى الاستدعاء
نوع المستحضر
سبب السحب
SFDA has issued a recall of two batches of Rozel due to the product is not comply with the requirements of the executive regulations for the Pharmaceutical establishments system.
التوصيات
For healthcare professionals:
- Stop dispensing the two batches of product immediately. Embargo/Quarantine all remaining stock. Affected batches should be returned to the supplier.
- 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 two batches may be reported to Saudi Vigilance either online or call center (Call 19999).
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