Recall 2 batches of SAXID 2MG TABLET
2026-02-12
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)
التصنيف
ملف
التاريخ
2025-09-07
اسم المستحضر
SAXID 2MG TABLET
اجراء الاستدعاء
مستوى الاستدعاء
نوع المستحضر
سبب السحب
The SFDA has issued a recall of two batches of SAXID 2 mg tablets due to noncompliance with the pre-specified specifications
التوصيات
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).
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