China NMPA Product Recall - Hot compress

Anhui Jintai Medical Device Co., Ltd. initiated a voluntary recall of its heating patch product after identifying a specific batch as substandard. The recall, indexed by the National Medical Products Administration (NMPA) as JGXX-2022-10117, was publicly announced on May 20, 2022, via the Anhui Provincial Drug Administration website. The affected product carries batch number 20210901 and is registered under Anhui Medical Device Registration No. 20192090181. The decision to recall was prompted by the company's internal findings that these particular heating patches did not meet established quality standards. This action aligns with regulatory expectations set forth by the NMPA, which oversees medical device safety and quality within China. While specific details regarding the nature and level of the recall, along with models and specifications, are outlined in an accompanying "Medical Device Recall Event Report Form," the primary issue centers on the product's failure to meet required quality benchmarks. Anhui Jintai Medical Device Co., Ltd. is taking proactive steps to address the quality issue and ensure patient safety.