Recall one batch of NEXOL 40 mg vial

Recall one batch of NEXOL 40 mg vial

2025-08-13

Product Description :

الاسم التجاري

الاسم العلمي

رقم التسجيل

رقم التشغيلة المتأثرة

الشركة الصانعة

trade name

scientific name

register number

affected batch number

manufacturer

NEXOL 40 MG VIAL

ESOMEPRAZOLE

3010222836

5BD014D

Tabuk Pharmaceutical Manufacturing Co.

Issue :

The Saudi Food and Drug Authority (SFDA) has issued a recall of one batch of NEXOL 40 MG VIAL due to non-compliance with the approved specifications. The affected batch is being voluntarily recalled by the company

Recommendations :

For healthcare professionals: Stop dispensing the affected batch immediately. Embargo/Quarantine all remaining stock. Affected batch should be returned to the supplier.

For patients,

  1. Consult your healthcare provider prior to discontinuing use of the affected batch, 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).