Recall one batch of NEXOL 40 mg vial
2026-02-05
الاسم التجاري الاسم العلمي رقم التسجيل رقم التشغيلة المتأثرة الشركة الصانعة trade name scientific name register number affected batch number manufacturer NEXOL 40 MG VIAL ESOMEPRAZOLE 3010222836 5BD014D Tabuk Pharmaceutical Manufacturing Co.
التاريخ
2025-08-13
اسم المستحضر
NEXOL 40 mg vial
اجراء الاستدعاء
مستوى الاستدعاء
نوع المستحضر
سبب السحب
The Saudi Food and Drug Authority (SFDA) has issued a recall of one batch of NEXOL 40 MG VIAL due to non-compliance with the approved specifications. The affected batch is being voluntarily recalled by the company
التوصيات
For healthcare professionals: Stop dispensing the affected 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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