Skip to main content

Recall of several batches of Combiwave 250,25 µg/ Pressurised inhalation product

2025-10-20

Product Description :

الاسم التجاري

الاسم العلمي

رقم التسجيل

رقم التشغيلة المتأثرة

الشركة الصانعة

Trade Name

Scientific Name

Register Number

Affected batch number

Manufacturer

Combiwave 250,25 µg/ Pressurised inhalation

Fluticasone Propionate, Salmeterol

1202256882

12250193B

12250232A

12250233A

12250332A

12250339A

12240471

12240771

12240772

12241372A

Glenmark Pharmaceuticals Limited-Baddi

Issue :

The Saudi Food and Drug Authority (SFDA) has issued a recall of several batches of the product Combiwave 250,25 µg/ Pressurised inhalation due to the batches’ non-compliance with the approved specifications of the product.

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 several batches of Combiwave 250,25 µg/ Pressurised inhalation product