China NMPA Product Recall - Medical centrifuge

On June 19, 2017, the National Medical Products Administration (NMPA) announced a voluntary product recall initiated by Beckman Coulter Trading (China) Co., Ltd. This action specifically targeted their medical centrifuges, identified under Registration No. 20140256. The primary reason for this recall stemmed from the company's use of an expired registration certificate number for these medical devices. This instance of regulatory non-compliance necessitated the recall to ensure adherence to established product registration standards.The recall has been designated as Class III, a classification indicating that the use of or exposure to the violative product is not likely to cause adverse health consequences. Beckman Coulter Trading (China) Co., Ltd. is responsible for implementing this voluntary recall. Comprehensive details regarding the specific models, specifications, and batch numbers of the affected centrifuges are provided in an accompanying "Medical Device Recall Event Report Form," which serves as the official document outlining the scope of the recall.