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Voluntary Recall of two batches of Dopram100 MG /5ML produced by EUMEDICA PHARMACEUTIC ALS FRANCE Manufacturer

2025-11-02

Product 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,

  1. Consult your healthcare provider prior to discontinuing use of the affected batches, or for any health concerns.
  2. Contact the recalling firm or SFDA if you have any questions about the recall.
  3. 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).


Voluntary Recall of two batches of Dopram100 MG /5ML produced by EUMEDICA PHARMACEUTIC ALS FRANCE Manufacturer