Recall one Batch of ENDOMETRIN 100 mg Vaginal tablet
الاسم التجاري الاسم العلمي رقم التسجيل رقم التشغيلة المتأثرة الشركة الصانعة Trade Name Scientific Name Register Number Affected batch number Manufacturer ENDOMETRIN 100 mg Vaginal tablet PROGESTERONE 3010222853 AB210A Q PHARMAAB
<p dir="RTL" style="direction: ltr;"><span><span>Saudi FDA has issued a recall one batch of ENDOMETRIN 100 mg Vaginal tablet due to suspected presence of bacteria (Burkholderia) in a number of samples of the product. Q PHARMAAB is voluntarily recalling the affected batch. </span></span></p>
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<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>
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<li><span><span><span><span>Consult your healthcare provider prior to discontinuing use of the affected batch , or for any health concerns.</span></span></span></span></li>
<li><span><span><span><span>Contact the recalling firm or Saudi FDA if you have any questions about the recall.</span></span></span></span></li>
<li><span><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></span></li>
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