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Recall batches of SABRIL 500MG F.C.TAB

2023-07-21

Product Description :

 

الاسم التجاري

الاسم العلمي

رقم التسجيل

رقم التشغيلة المتأثرة

الشركة الصانعة

Trade Name

Scientific Name

Register Number

Affected batch number

Manufacturer

SABRIL 500MG F.C.TAB

Vigabatrin 500 Mg

25-883-19

2006B

2988D

2989A

2990D

sanofi-aventis

Issue :

Saudi FDA issued Recall four batches of SABRIL 500MG F.C.TAB due to) Tiapride (cross Contamination. Sanofi-Aventis is voluntarily recalling the affected batches.

Recommendations :

For healthcare professionals, Stop dispensing the above batches 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 batches, or for any health concerns.
  • Contact the recalling firm or Saudi FDA 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).


Recall batches of SABRIL 500MG F.C.TAB