Recall one batch of ZITOTEC 200mg
الاسم التجاري الاسم العلمي رقم التسجيل رقم التشغيلة المتأثرة الشركة الصانعة Trade Name Scientific Name Register Number Affected batch number Manufacturer ZITOTEC 200mg Misoprostol Unregistered GKC1864A Sun Pharma Laboratories ITD. India
<p><span><span>Saudi FDA has issued a recall of one batch of ZITOTEC 200mg due to the batch did not comply with the necessary technical requirements.</span></span></p>
<p><span><span><strong><span>For healthcare professionals: </span></strong><span>Stop dispensing the above batch immediately. Embargo/Quarantine all remaining stock. Affected batch should be returned to the supplier.</span></span></span></p>
<p><span><span><strong><span>For patients,</span></strong></span></span></p>
<ol>
<li><span><span><span>Consult your healthcare provider prior to discontinuing use of the affected batch , or for any health concerns.</span></span></span></li>
<li><span><span><span>Contact the recalling firm or SFDA if you have any questions about the recall.</span></span></span></li>
<li><span><span><span>Adverse reactions or quality problems experienced with the use of this product may be reported to </span><a href="https://ade.sfda.gov.sa/"><span>Saudi Vigilance</span></a><span> either online or call center (Call 19999).</span></span></span></li>
</ol>
Comments and Suggestions
For any inquiries or comments about the government services, please fill in the required information.