Recall two batches of NEUPOGEN 30 MU
2026-02-12
الاسم التجاري الاسم العلمي رقم التسجيل رقم التشغيلة المتأثرة الشركة الصانعة Trade Name Scientific Name Register Number Affected batch number Manufacturer NEUPOGEN 30 MU FILGRASTIM 1107245543 1193771A 1193772A AMGEN MANUFACTURING LIMITED
التصنيف
ملف
التاريخ
2025-12-25
اسم المستحضر
NEUPOGEN 30 MU
اجراء الاستدعاء
مستوى الاستدعاء
نوع المستحضر
سبب السحب
The Saudi Food and Drug Authority (SFDA) has issued a recall of two batches of the NEUPOGEN 30 MU product due to non-compliance with the approved product specifications.
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).
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