China NMPA Product Recall - Hot compress

Anhui Jintai Medical Device Co., Ltd. has issued a voluntary Level III recall for its heating patches, specifically those manufactured under batch number 20210824. This critical action was prompted by the product's failure to meet established quality standards during a routine random inspection. While the exact date of this inspection is not detailed in the available document, the National Medical Products Administration (NMPA) officially publicized the recall on July 14, 2022. The Level III classification for this recall indicates that the product defect is unlikely to cause adverse health consequences, but corrective action is still necessary to maintain product integrity and public trust. Under the regulatory oversight of the NMPA, Anhui Jintai Medical Device Co., Ltd. is undertaking this recall to address the identified quality deviation and prevent potential issues. The company is required to remove all affected heating patches from distribution and the market. Stakeholders seeking comprehensive information regarding the specific models, specifications, and affected batches are directed to the 'Medical Device Recall Events' section on the NMPA website. This proactive measure by Anhui Jintai Medical Device Co., Ltd. demonstrates adherence to regulatory requirements and a commitment to ensuring the quality and safety of medical devices supplied to consumers, as mandated by the NMPA framework.