China NMPA Product Recall - Disposable sterile syringe with needle

On October 19, 2021, Yunnan Haodi Medical Device Co., Ltd. initiated a Class III voluntary recall for its disposable sterile syringes with needles. This action, reported by the company and published by the National Medical Products Administration (NMPA) and the Yunnan Provincial Drug Administration, was prompted by the product's non-compliance with established regulations governing medical device operations. While no specific inspection dates are provided in this announcement, the recall addresses a detected deviation from regulatory standards. The core issue involves a general non-adherence to the operational requirements for medical devices, which are critical for ensuring product quality and patient safety. As a required measure, Yunnan Haodi Medical Device Co., Ltd. is voluntarily withdrawing the affected syringes from distribution. Further comprehensive details concerning the specific models, specifications, and batch numbers of the recalled products are documented in a separate Medical Device Recall Event Report Form. This proactive step highlights the company’s responsibility in maintaining regulatory compliance and upholding the integrity of medical products.