China NMPA Product Recall - Soft tissue circumcision knife

Noboco Trading (Shanghai) Co., Ltd. initiated a voluntary Class III recall of its soft tissue circumcision knives, as announced by the National Medical Products Administration (NMPA) on August 29, 2017. The recall was prompted by discrepancies identified on the product's Chinese label. Specifically, the registrant's name and registered address printed on the label were found to be inconsistent with the information officially recorded on the product's registration certificates (National Food and Drug Administration Import Medical Device Registration No. 20122060740 and National Medical Device Registration No. 20152062936). This issue falls under the regulatory oversight of the NMPA, which is responsible for ensuring the accuracy and compliance of medical device information in China. Although the document does not specify inspection dates, the recall itself serves as a corrective action taken by the company to address a labeling non-conformity. The primary required action by Noboco Trading (Shanghai) Co., Ltd. was to execute this voluntary recall to rectify the misleading label information, with detailed product specifics found in an attached recall event report form.