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Recently, the State Food and Drug Administration issued an announcement stating that in accordance with the relevant provisions of Article 83 of the Drug Administration Law of the People's Republic of China, the State Drug Administration organized a post-marketing evaluation of Lianbizhi injection
.
After evaluation, the State Drug Administration decided to stop the production, sales and use of Lianbizhi injection in China from now on, and cancel the drug registration certificate
.
For products that have been marketed, the holder of the drug marketing authorization is responsible for the recall, and the recalled products are supervised and destroyed by the local provincial drug supervision and administration department or take other measures such as harmless treatment in accordance with the law
.