China NMPA Product Recall - diamond needle

Guangzhou Xifu Medical Equipment Co., Ltd. has initiated a voluntary Class III recall for its diamond needles, following a self-inspection that identified a critical labeling deficiency. The company discovered that some product labels did not clearly indicate the production and expiration dates, which are essential for product traceability and safety. This recall falls under the regulatory framework of the National Medical Products Administration (NMPA) and was reported through the Guangdong Provincial Drug Administration. As a required action, Guangzhou Xifu Medical Equipment Co., Ltd. is actively retrieving all affected diamond needle products from the market. The specific models, specifications, and batches subject to this recall are detailed in a supplementary Medical Device Recall Event Report Form. This measure underscores the company's commitment to addressing regulatory non-compliance and ensuring the integrity and proper identification of its medical devices, thereby safeguarding user confidence and adhering to established industry standards.