Recall 2 batches of SAXID 2MG TABLET
2025-09-07Product Description :
|
الاسم التجاري |
الاسم العلمي |
رقم التسجيل |
رقم التشغيلة المتأثرة |
الشركة الصانعة |
|
Trade Name |
Scientific Name |
Register Number |
Affected batch number |
Manufacturer |
|
SAXID 2MG TABLET |
RISPERIDONE |
76-171-11 |
2310114 2312023 |
The Jordanian Pharmaceutical Manufacturing Medical Equipment Co. Ltd. (JPM) |
Issue :
The SFDA has issued a recall of two batches of SAXID 2 mg tablets due to noncompliance with the pre-specified 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,
- 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).