Recall some batches of LINZESS products
2024-07-14
الاسم التجاري الاسم العلمي رقم التسجيل رقم التشغيلة المتأثرة الشركة الصانعة Trade Name Scientific Name Register Number Affected batch number Manufacturer LINZESS 290 µg LINACLOTIDE Unregistered 1173604 Forest Laboratories Ireland Limited A2022020 LINZESS 145 µg 1173004 A2022016
<p><span><span><span>SFDA has issued a recall some batches of LINZESS products due to the affected batches are not comply with the required technical specifications. abbvie is voluntarily recalling the above batches.</span></span></span><span dir="RTL" lang="AR-SA"><span> </span></span></p>
<p><span><span><strong><span>For healthcare professionals: </span></strong><span>Stop dispensing the affected batches immediately. Embargo/Quarantine all remaining stock. Affected batches 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 batches, 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>
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