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Recall 2 batches of SAXID 2MG TABLET

2025-09-07

Product 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,

  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 2 batches of SAXID 2MG TABLET