Voluntary Recall of two batches of Dopram100 MG /5ML produced by EUMEDICA PHARMACEUTIC ALS FRANCE Manufacturer
2025-11-02Product Description :
|
الاسم التجاري |
الاسم العلمي |
رقم التسجيل |
رقم التشغيلة المتأثرة |
الشركة الصانعة |
|
Trade Name |
Scientific Name |
Register Number |
Affected batch number |
Manufacturer |
|
Dopram 100 MG /5ML |
DOXAPRAM |
غير مسجل |
50478 50293 |
EUMEDICA PHARMACEUTIC ALS FRANCE |
Issue :
SFDA has issued a recall of two batches of Dopram 100 MG /5ML due to non-compliance with specifications. The company requested voluntary recall of the affected batches.
Recommendations :
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).