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国家药品监督管理局1999年初通知，外科整形用品，乌克兰英捷尔法勒公司生产的亲水性聚丙烯酸胺凝胶自1997年12月在我国注册审查上市以来，以「国药器监（进）字97第1252号〕所批产品的来源及医生的资格都未经认定。一些用户反映使用该产品后对身体造成了不良影响。经组织专家
Since the State Drug Administration informed in early 1999 that since the plastic surgery products and the hydrophilic polyacrylamide gels manufactured by the British company Agfa in Ukraine have been registered and reviewed in China since December 1997, 97 No. 1252] The origin of the products approved and the qualifications of the medical practitioners have not been validated, and some users have reported that the use of this product has adversely affected the health of the patients.