Recall of batches manufactured using active ingredients sourced from NECTAR LIFE SCIENCES LIMITED
الاسم التجاري الاسم العلمي رقم التسجيل رقم التشغيلة المتأثرة الشركة الصانعة Trade Name Scientific Name Register Number Affected batch number Manufacturer Cefuzime 500 mg FCT CEFUROXIME AXETIL 1809222615 08483 09379 09886 09885 08481 Gulf Pharmaceutical Industries (Julphar) Cefuzime 500 MG TAB CEFUROXIME AXETIL 0210222682 08490 08759 08476 09683...
التصنيف
ملف
التاريخ
2025-11-05
اسم المستحضر
مستحضرات مصنع NECTAR LIFE SCIENCES LIMITED
اجراء الاستدعاء
مستوى الاستدعاء
نوع المستحضر
سبب السحب
The SFDA has issued a recall of batches manufactured using active ingredients sourced from NECTAR LIFE SCIENCES LIMITED. It has been determined that NECTAR LIFE SCIENCES LIMITED failed to comply with Good Manufacturing Practices (GMP), which may affect the safety and quality of products manufactured using active ingredients from this manufacturer.
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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