China NMPA Product Recall - Disposable infusion set with needle

Yunnan Haodi Medical Device Co., Ltd. initiated a voluntary Class III recall of its disposable infusion sets with needles, as reported by the National Medical Products Administration (NMPA) and the Yunnan Provincial Drug Administration on October 19, 2021. The primary reason for this recall stems from the discovery of inaccurate and false labeling and markings on these medical devices. The affected product, identified by Registration No.: 20163660604, is subject to this action to ensure patient safety and product integrity. This recall highlights the company's commitment to regulatory compliance and product quality. Specific details regarding the models, specifications, and batch numbers of the impacted products are available in the "Medical Device Report Form." The NMPA, the governing body, oversees such regulatory actions to uphold public health standards and ensure medical device reliability within China.