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Recall of Fasenra Pen 30 mg/mL Batch

2025-12-29

Product Description :

الاسم التجاري

الاسم العلمي

رقم التسجيل

رقم التشغيلة المتأثرة

الشركة الصانعة

Trade Name

Scientific Name

Register Number

Affected batch number

Manufacturer

Fasenra pen 30MG/ML

Benralizumab

0212222960

YK0060

AstraZeneca Pharmaceuticals LP

Issue :

The Saudi Food and Drug Authority (SFDA) has issued a recall for one batch of the Fasenra Pen 30 mg/mL product due to its non-compliance with the approved product specifications.

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).


Recall of Fasenra Pen 30 mg/mL Batch