Product Description :

Issue :

SFDA has issued a recall batches of SIFROL 0.18 MG , SIFROL 0.7MG due to non-compliance with required specifications.

Recommendations :

For healthcare professionals, Stop dispensing the above 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 Saudi FDA 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).