China NMPA Product Recall - Disposable vacuum blood collection tubes

On September 2, 2019, Jiangxi Changqing Medical Technology Co., Ltd. initiated a voluntary Class III recall for its disposable vacuum blood collection tubes. This action was taken following the identification of quality defects within these medical devices, which were found to compromise the accuracy of test results. The company reported this issue to the National Medical Products Administration (NMPA), the regulatory body overseeing medical products in China. While no specific inspection dates were provided, the recall commenced in response to these identified product deficiencies. The required action involves the systematic removal of the affected disposable vacuum blood collection tubes, specifically those registered under Certificate No. Ganxiezhuzhun 20142410352, from circulation. Detailed information regarding the implicated product models, specifications, and batch numbers can be found in the "Medical Device Recall Event Report Form" provided by the company. This recall underscores Jiangxi Changqing Medical Technology Co., Ltd.'s commitment to ensuring product quality and compliance with NMPA regulations, aiming to safeguard the reliability of medical diagnostics.