Recall of all batches from the product: NOREPIRIN 2 mg/ml Injection
2026-10-12
الاسم التجاري الاسم العلمي رقم التسجيل رقم التشغيلة المتأثرة الشركة الصانعة Trade Name Scientific Name Register Number Affected batch number Manufacturer NOREPIRIN 2 mg/ml Injection NOREPINEPHRINE BITARTRATE 1303245047 جميع التشغيلات Huons Co. Ltd Korea
التصنيف
Health practitioners
التاريخ
2026-10-07
اسم المستحضر
NOREPIRIN 2 mg/ml Injection
نوع المستحضر
Medicine Product
اجراء الاستدعاء
Wholesale level
مستوى الاستدعاء
Hospital level
سبب السحب
SFDA has issued a recall of all batch from the product: NOREPIRIN 2 mg/ml Injection Based on Decision No. 48/SFDA/1274/105 of the Committee for the Registration of Pharmaceutical Companies, Manufacturers, and Their Products, the manufacturer's registration has been suspended and all its products recalled due to critical observations concerning data integrity and aseptic processing..
التوصيات
For healthcare professionals: Stop dispensing the 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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