Recall 2 batches of ATROVENT 500MCG-2ML UDV (SOLUTION FOR INHALATION)
الاسم التجاري الاسم العلمي رقم التسجيل رقم التشغيلة المتأثرة الشركة الصانعة Trade Name Scientific Name Register Number Affected batch number Manufacturer ATROVENT 500MCG-2ML UDV (SOLUTION FOR INHALATION) IPRATROPIUM BROMIDE 106-68-16 3982202D2 3982202D1 Laboratoire Unither
التصنيف
ملف
التاريخ
2025-05-19
اسم المستحضر
ATROVENT 500MCG-2ML UDV
اجراء الاستدعاء
مستوى الاستدعاء
نوع المستحضر
سبب السحب
SFDA has issued a recall of two batches of ATROVENT 500MCG/2ML UDV due to discrepancies in the expiration dates printed on the outer packaging of the product
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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