Recall of one batch of VISIPAQUE 320mg/mL
2026-04-20
الاسم التجاري الاسم العلمي رقم التسجيل رقم التشغيلة المتأثرة الشركة الصانعة Trade Name Scientific Name Register Number Affected batch number Manufacturer VISIPAQUE 320MG/ML IODIXANOL 39-315-12 17303283 GE HEALTHCARE
التصنيف
ملف
التاريخ
2026-04-05
اسم المستحضر
VISIPAQUE 320mg/mL
اجراء الاستدعاء
مستوى الاستدعاء
نوع المستحضر
سبب السحب
SFDA has issued a recall of one batch of VISIPAQUE 320mg/mL due to presence of dark particles adhered inside the bottle, which may affect the safety and quality of the product.
التوصيات
For healthcare professionals: Stop dispensing the affected batch 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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