Recall of several batches of Combiwave 250,25 µg/ Pressurised inhalation product
2025-10-20Product 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,
- Consult your healthcare provider prior to discontinuing use of the affected batches, or for any health concerns.
- Contact the recalling firm or SFDA 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).